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Sponsored by: |
Atrium Medical Center |
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Information provided by: | Atrium Medical Center |
ClinicalTrials.gov Identifier: | NCT00206193 |
The purpose of this study is to determine which medical treatment is the most effective to terminate a pregnancy.
Condition | Intervention | Phase |
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Abortion, Induced |
Drug: mifepristone Drug: misoprostol Drug: sulprostone |
Phase II |
Study Type: | Observational |
Study Design: | Prospective |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Female |
Inclusion Criteria:
Exclusion Criteria:
Contact: Suzanne HW Vonken, Dr. | 003145-5766666 ext 466825 | svonken@gmail.com |
Contact: F Roumen, Dr. | 003145-5766666 ext 466509 |
Netherlands, Limburg | |
Atrium Medisch Centrum | Recruiting |
Heerlen, Limburg, Netherlands | |
Contact: Suzanne HW Vonken, Dr. 045-5766666(6825) | |
Principal Investigator: Suzanne HW Vonken, Dr. |
Study Director: | F Roumen, Dr. | Atrium Medisch Centrum Heerlen |
Study ID Numbers: | TOP-protocol |
Study First Received: | September 13, 2005 |
Last Updated: | October 29, 2007 |
ClinicalTrials.gov Identifier: | NCT00206193 |
Health Authority: | United States: Food and Drug Administration |
termination of pregnancy |
Misoprostol Mifepristone Sulprostone |
Abortifacient Agents, Steroidal Contraceptives, Postcoital, Synthetic Oxytocics Contraceptive Agents Hormone Antagonists Contraceptives, Oral Physiological Effects of Drugs Gastrointestinal Agents Contraceptive Agents, Female Hormones, Hormone Substitutes, and Hormone Antagonists |
Reproductive Control Agents Abortifacient Agents, Nonsteroidal Contraceptives, Postcoital Luteolytic Agents Pharmacologic Actions Therapeutic Uses Anti-Ulcer Agents Abortifacient Agents Menstruation-Inducing Agents Contraceptives, Oral, Synthetic |