Track topics on Twitter Track topics that are important to you
High blood pressure (BP) before pregnancy is called chronic hypertension (CHTN), and is associated with an increased risk of development of pregnancy related high BP called preeclampsia, preterm delivery, decreased growth of the fetus, fetal death, premature separation of the placenta from the uterus resulting in damage to the fetus and cesarean delivery. Longer duration and severity of CHTN in pregnancy leads to worse outcomes for the mother and the fetus. Treatment of mild CHTN in pregnancy does not improve these outcomes, and therefore, medications to lower BP are used for moderate to severe hypertension. To date the literature on the medications used in pregnancy is extremely limited.
Methyldopa is used as a first choice medicine for CHTN in pregnancy. It acts on the central nervous system (CNS) by relaxation of the blood vessels leading to a decrease in BP. It does not decrease the blood flow to the uterus, placenta, or the fetus (4). Methyldopa is a weak antihypertensive medicine given three or four times a day and frequently needs changes in the dose or may require an additional medication to control BP. This may lead to a greater chance of non compliance. Another option is Clonidine which is an effective antihypertensive treatment and is available in many forms (oral, parenteral, and transdermal.) It acts on the maternal CNS. Clonidine is not associated with teratogenic or neonatal side effects. Transdermal clonidine (catapres-TTS®) is a preparation of clonidine hydrochloride that can be released and absorbed transdermally over a 7-day period.
The study will determine differences in compliance between the two antihypertensive regimens- oral methyldopa and Catapres-TTS, comparisons of patient tolerability, compliance and adequacy of BP control, as well as provide information on an alternate option for BP control.
Purpose of the Study:
The purpose of this of open-label randomized clinical trial is to compare clonidine patch (Catapres-TTS®) and orally administered methyldopa (Aldomet®) over a 4-week period for compliance in pregnant women between 14 and 28 weeks of gestation. In addition, this study will evaluate blood pressure (BP) control, patient tolerability, and development of side effects to each medication. Patients will be alternately randomized to receive methyldopa (standard of care) or clonidine patch.
Clonidine is an effective antihypertensive agent with similar mechanism of action to methyldopa. Transdermal clonidine may provide a better compliance profile, adequate BP control and, therefore, may be used as an alternative to methyldopa for the treatment of CHTN in pregnancy.
Primary outcome of the study is patient compliance. Compliance will be measured via patient diary, promptness of keeping appointments, and pill/patch counts at each visit. Overall compliance will be calculated over a 4 week study period by adding compliance points for each visit as outlined in the data sheet.
Secondary outcomes are:
1. Change in mean arterial BP at weeks 1,2,3,4 in comparison to baseline BP at the initial visit (It will be used in patients newly started on medications or in patients with uncontrolled BP at baseline).
2. Side effects to each medication as reported by the patients.
Background and Significance
Chronic hypertension (CHTN) affects 1-5% of pregnancies. It is defined as BP of 140/90 or higher before the 20th week of gestation or beyond 12 weeks postpartum. CHTN is associated with an increased risk of preeclampsia, preterm delivery, intrauterine growth restriction, intrauterine fetal demise, placental abruption and cesarean delivery. Mild hypertension is defined as BP < 150/100 mm Hg and severe hypertension as BP > 160/110 mm Hg. There is a direct correlation of adverse perinatal outcomes with duration and severity of CHTN in pregnancy. Treatment of mild CHTN in pregnancy does not improve perinatal outcomes, and therefore, antihypertensive therapy is reserved for moderate to severe hypertension only.
Methyldopa is used as a first line therapy for CHTN in pregnancy. It is a central alpha-adrenergic agonist that decreases peripheral sympathetic outflow and thus results in a decrease in peripheral resistance and BP. It does not impact uteroplacental blood flow and fetal hemodynamics. Methyldopa is a weak antihypertensive agent and often times there is a need for increase in dose, frequency and/or addition of another medication to optimize BP control with advancing gestational age. Side effects of methyldopa include sedation, orthostatic hypotension, edema, weight gain, bradycardia, and dry mouth. Rarely, aggravation of angina, congestive heart failure, pancreatitis, colitis, hyperprolactinemia, bone marrow depression, hemolytic anemia, false positive anti-nuclear antibodies and rheumatoid factor may be seen.
The use of various classes of antihypertensive medications in pregnancy is limited due to potential teratogenic effects. Angiotensin converting enzyme inhibitors are contraindicated in pregnancy. The use of beta-blockers and diuretics is controversial, and there is limited data on calcium channel blockers in pregnancy.
Clonidine is an effective antihypertensive treatment and is available in oral, parenteral, and transdermal dosage forms. Although oral and parenteral forms are commonly employed for short-term use in hypertensive urgencies, data regarding its use in pregnancy are lacking. It acts by stimulating α2-adrenergic receptors in the central nervous system (CNS), which depresses peripheral sympathetic nervous system outflow, and thus lowering BP. Clonidine is not associated with teratogenic effects in the fetus. Reproduction studies performed in rabbits at doses up to 3 times the maximum recommended daily human dose (MRDHD) of clonidine hydrochloride have revealed no evidence of teratogenic or embryotoxic potential. The pharmacokinetics of clonidine in pregnancy has been studied. Clonidine crossed placenta and fetal concentration is 0.89 of the maternal level. No neonatal side effects have been reported. Clonidine is metabolized by the liver and is excreted unchanged in the urine.
Therapeutic levels of orally administered drugs are affected by the transit time through small intestines and the presence of food and liquid in the gastrointestinal tract. Transdermal administration of drugs by passes the first-pass metabolism through the liver, requires smaller dose to achieve therapeutic effects, and promotes patient compliance. In addition, the drug is absorbed through the skin at a constant rate eliminating peak and troughs associated with oral administration. This may result in steadier BP control with transdermal clonidine administration. This may be of benefit in pregnancy as the gastrointestinal transit time is significantly prolonged due to progesterone effects and nausea vomiting in the first trimester may limit the use of orally administered drugs. In addition, one would expect improved patient compliance be avoiding repeated dosing such as four times a day schedule for methyldopa.
Transdermal clonidine (Catapres-TTS®) is a preparation of clonidine hydrochloride that can be released and absorbed transdermally over a 7-day period. Its side effect profile is similar to methyldopa including tiredness, lethargy, drowsiness, constipation and dry mouth. Orthostatic hypotension occurs in 3% patients with oral administration and has not been reported with the transdermal form. Skin reactions including redness, itching, and darkening of the skin may occur with clonidine patches. Rarely, angioedema, atrioventricular block, chest pain, congestive heart failure, hepatitis, thrombocytopenia, or urinary retention may occur.
A study of hypertension in non-pregnant individuals from United Kingdom showed that only 40% of patients who were started on a new antihypertensive drug were compliant six months later. There are no data available on compliance with antihypertensive medications in pregnancy, although our anecdotal experience is of improved compliance with medications in pregnancy compared to a non-pregnant state.
Our study will determine differences in compliance between the two antihypertensive drugs, and will provide additional comparisons of patient tolerability and adequacy of BP control. This may be of particular value in pregnant women who are unable to tolerate oral feeds e.g. those with hyperemesis gravidarum, or in immediate postoperative period. In addition, it will provide information on an alternate option for BP control, which has not been described in obstetrical literature.
1. National High Blood Pressure Educational Program Working Group. Report on High Blood Pressure in Pregnancy. Am J Obstet Gynecol 1990;163:1691-1712.
2. Report of the National High Blood Pressure Education Program Working Group on High Blood Pressure in Pregnancy. Am J Obstet Gynecol 2000;183:S1-S22.
3. Chronic Hypertension in Pregnancy. ACOG Practice Bulletin No. 29. American College of Obstetricians and Gynecologists. Obstet Gynecol 2001;98:177-185.
4. Montan S, Anandakumar C, Arulkumaran S, Ingemarsson I, Ratnam SS. Effects of Methyldopa on Uteroplacental and Fetal Hemodynamics in Pregnancy Induced Hypertension. Am J Obstet Gynecol 1993;168:152-6.
5. Horrath JS, Phippard A, Korda A, Hendersen-Sart DJ, Child A, Tiller DJ. Clonidine Hydrochloride - A Safe and Effective Antihypertensive in Pregnancy. Obstet Gynecol 1985;66:634-8.
6. Turnbull AC, Ahmad S. Catapress in the Treatment of Hypertension in Pregnancy, A Preliminary Study. In Hypertension. Symposium of the Royal College of Surgeons, London 1970:237-45
7. Hartikainen-Sorri AL, Heikkinen JE, Koivisto M. Pharmacokinetics of Clonidine During Pregnancy and Nursing. Obstet Gynecol 1987;69:598-600.
8. Ala-Kokko TI, Pienimaki P, Lampela E, Hollmen AI, Pelkonen O, Vahakangas K. Transfer of Clonidine and Dexmedetrmidine Across the Isolated Perfused Human Placenta. Acta Anesthesiol Scand 1997;41(2):313-19.
9. Jones JK, Gorkin L, Lian JF, Staffa JA, Fletcher AP. Discontinuation of and Changes in Treatment after start of new courses of Antihypertensive Drugs: A Study of a United Kingdom Population. BMJ 1995;311:293-5
Allocation: Randomized, Control: Active Control, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
methyldopa vs. clonidine, clonidine patch
Long Beach Memorial Medical Center
University of California, Irvine
Published on BioPortfolio: 2014-08-27T03:44:27-0400
The purpose of this study is to determine the pharmacokinetic dose proportionality of 50 μg and 100 μg Clonidine and comparative bioavailability of clonidine with that from the Reference...
The goal of this study is to confirm that levetiracetam has a better tic-suppressing profile than that of the widely used tic-suppressing medication, clonidine. More specifically, we hypo...
People with heart failure often have weakness in their leg muscles. This study will determine whether the leg weakness is due to very high adrenaline levels and whether the medication clon...
The use of increasing doses of clonidine plus bupivacaine in caudal anesthesia provides better postoperative analgesia than bupivacaine alone after hypospadia's surgery.
This is a study of the effects of clonidine: how it affects responses to stress and to things that remind people of drugs. Clonidine is being compared to placebo. Participants listen to ...
Nonselective beta blockade (BB) and clonidine may abrogate catecholamine-mediated persistent injury-associated anemia. We hypothesized that critically ill trauma patients who received BB or clonidine ...
To examine whether adding clonidine to the morphine regimen for treatment of neonatal abstinence syndrome (NAS) is associated with a shorter length of treatment compared to morphine alone.
The diagnosis of growth hormone deficiency (GHD) is currently based on clinical, auxological, biochemical, and neuro-radiological investigation. Provocative tests of GH secretion using physiological/p...
The aims of this study were to determine if it is possible to truncate a combined simultaneous arginine clonidine stimulation test, and to correlate the outcome of the test with clinical indices of GH...
Pharmacopuncture with Scolopendra subspinipes suppresses mechanical allodynia in oxaliplatin-induced neuropathic mice and potentiates clonidine-induced anti-allodynia without hypotension or motor impairment.
Chemotherapy-induced neuropathic pain is a common dose-limiting side effect of anticancer drugs but lacks an effective treatment strategy. Scolopendra subspinipes (SS) has been used in traditional med...
An alpha-2 adrenergic agonist that crosses the blood-brain barrier. Clonidine acts centrally by reducing sympathetic tone, resulting in a fall in diastolic and systolic blood pressure and a reduction in heart rate. It also acts peripherally, and this peripheral activity may be responsible for the transient increase in blood pressure seen during rapid intravenous administration. (From Martindale, the Extra Pharmacopoeia, 30th ed, p350)
A nonselective alpha-adrenergic antagonist. It is used in the treatment of hypertension and hypertensive emergencies, pheochromocytoma, vasospasm of RAYNAUD DISEASE and frostbite, clonidine withdrawal syndrome, impotence, and peripheral vascular disease.
Receptors of CLONIDINE and other IMIDAZOLINES. Activity of the ligands was earlier attributed to ADRENERGIC ALPHA-2 RECEPTORS. Endogenous ligands include AGMATINE, imidazoleacetic acid ribotide, and harman.
An electrophysiologic technique for studying cells, cell membranes, and occasionally isolated organelles. All patch-clamp methods rely on a very high-resistance seal between a micropipette and a membrane; the seal is usually attained by gentle suction. The four most common variants include on-cell patch, inside-out patch, outside-out patch, and whole-cell clamp. Patch-clamp methods are commonly used to voltage clamp, that is control the voltage across the membrane and measure current flow, but current-clamp methods, in which the current is controlled and the voltage is measured, are also used.
A subclass of alpha-adrenergic receptors (RECEPTORS, ADRENERGIC, ALPHA). alpha-2 Adrenergic receptors can be pharmacologically discriminated, e.g., by their high affinity for the agonist clonidine and the antagonist yohimbine. They are found on pancreatic beta cells, platelets, and VASCULAR SMOOTH MUSCLE, as well as both pre- and postsynaptically in the central and peripheral nervous systems.
Obstetrics and gynaecology
Fertility Menopause Obstetrics & Gynaecology Osteoporosis Women's Health Obstetrics and gynaecology comprises the care of the pregnant woman, her unborn child and the management of diseases specific to women. Most consultant...
The United States Food and Drug Administration (FDA) has approved on October 8th 2013 Adempas® (riociguat) tablets for: (i) the treatment of adults with persistent/recurrent chronic thromboembolic pulmonary hypertension (CTEPH) (WHO* Group 4) after ...