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| Sponsor: | Hospices Civils de Lyon |
|---|---|
| Information provided by: | Hospices Civils de Lyon |
| ClinicalTrials.gov Identifier: | NCT00127075 |
Purpose
Multiple sclerosis (MS) affects 1 in 1000 people in western countries, mainly women in their childbearing years. It is an autoimmune disease of the central nervous system (CNS), which results in a chronic focal inflammatory response with subsequent demyelination and axonal loss. Recent prospective studies reported a significant decline by two-thirds in the rate of relapses during the third trimester of pregnancy and a significant increase by two-thirds during the first three months post-partum by comparison to the relapse rate observed during the year prior to the pregnancy (Confavreux et al., 1998). These dramatic changes in the relapse rate occur at a time when the impregnation of many substances (among which, sexual steroids) is at its highest, before a dramatic decline to the pre-pregnancy levels, immediately following delivery.
It may be hypothesized that sexual steroids could exert beneficial effects through a modulation of the immune state with a lowering of the pro-inflammatory lymphocyte responses of the Th1 type and an enhancement of the anti-inflammatory responses of the Th2 type. They may also play a direct role in the remyelination of central nervous system lesions, as they do in the peripheral nervous system. The POPART'MUS study is a European, multicentre, randomized, placebo-controlled and double-blind clinical trial, which aims to prevent MS relapses related to the post-partum condition, by administering high doses of progestin (nomegestrol acetate), in combination with endometrial protective doses of estradiol. Treatment will be given immediately after delivery and continuously during the first three months post-partum. Assuming the results of the trial to be positive, this new treatment could be considered in the relapsing-remitting phase of the disease in women afar from pregnancy and post-partum.
| Condition | Intervention | Phase |
|---|---|---|
|
Multiple Sclerosis |
Drug: nomegestrol acetate Drug: estradiol |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator), Placebo Control, Parallel Assignment |
| Official Title: | POPART'MUS: Prevention of Post Partum Relapses With Progestin and Estradiol in Multiple Sclerosis |
| Estimated Enrollment: | 300 |
| Study Start Date: | June 2005 |
Eligibility| Ages Eligible for Study: | 18 Years to 50 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| France | |
| Hôpital Pierre Wertheimer | Recruiting |
| BRON, France, 69677 | |
| Contact: Iuliana Achiti, MD +33 4 72 68 13 17 popartmus@edmus.org | |
| Principal Investigator: Christian Confavreux, MD | |
| Principal Investigator: | Christian Confavreux, MD | Hospices Civils de Lyon |
More Information
| Study ID Numbers: | 2004.363 |
| Study First Received: | August 4, 2005 |
| Last Updated: | October 4, 2007 |
| ClinicalTrials.gov Identifier: | NCT00127075 History of Changes |
| Health Authority: | France: Afssaps - French Health Products Safety Agency |
|
Multiple sclerosis. Relapses. Post partum. Pregnancy. Delivery. Hormones. Progesterone. Estradiol. Clinical trial. Prevention. |
|
Disease Attributes Contraceptive Agents Estradiol valerate Physiological Effects of Drugs Contraceptive Agents, Female Hormones, Hormone Substitutes, and Hormone Antagonists Estradiol 17 beta-cypionate Reproductive Control Agents Hormones Pathologic Processes Multiple Sclerosis Estradiol 3-benzoate Progestins |
Therapeutic Uses Polyestradiol phosphate Autoimmune Diseases of the Nervous System Estrogens Autoimmune Diseases Immune System Diseases Demyelinating Diseases Nervous System Diseases Sclerosis Estradiol Recurrence Pharmacologic Actions Demyelinating Autoimmune Diseases, CNS |