Abortion, Induced Clinical Trial
| NCT number | NCT00206193 |
| Other study ID # | TOP-protocol |
| Secondary ID | |
| Status | Recruiting |
| Phase | Phase 2 |
| First received | September 13, 2005 |
| Last updated | October 29, 2007 |
The purpose of this study is to determine which medical treatment is the most effective to terminate a pregnancy.
| Status | Recruiting |
| Enrollment | 0 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | |
| Gender | Female |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Pregnant women by whom a termination of pregnancy is desired. Exclusion Criteria: - Women with liver/kidney disease - Women on long-term use of corticosteroids (> 6 months) - Cardiovascular problems - Therapy-resistant diabetic women - Therapy-resistant asthma/bronchitis - Thalassemia - Ulcerative colitis - Peptic ulcer disease - Glaucoma - Porphyria - Allergic reaction to prostaglandin or mifepristone - Women with a prior caesarian section or women with contractions at the start of the study |
Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| Netherlands | Atrium Medisch Centrum | Heerlen | Limburg |
| Lead Sponsor | Collaborator |
|---|---|
| Atrium Medical Center |
Netherlands,
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT01541293 -
Intrauterine Lidocaine for Laminaria
|
Phase 1 | |
| Completed |
NCT00177333 -
Serum Levels of Doxycycline at the Time of Abortion With Two Dosing Regimens
|
Phase 4 | |
| Completed |
NCT00370487 -
Comparison of the Safety of First Trimester Abortions Performed by Physicians and Non-Physicians in South Africa and Viet Nam.
|
N/A | |
| Completed |
NCT00188071 -
Postoperative Pain After Medical Abortion Under Local Anesthesia : Comparison of Several Analgesic Regimen
|
N/A | |
| Completed |
NCT02277249 -
Transvaginal Versus Transabdominal Digoxin Prior to Second-trimester Abortion
|
N/A | |
| Completed |
NCT00386867 -
A Randomized Trial of Buccal Compared to Oral Misoprostol Following Mifepristone for Medical Abortion up to 63 Days LMP
|
N/A | |
| Completed |
NCT00677755 -
Medical Abortion for Emergency Contraception Failure
|
N/A | |
| Completed |
NCT02279914 -
Misoprostol Dose and Timing Before Surgical Abortion at 13 to 16 Weeks' Gestation: a Randomized Trial
|
N/A | |
| Completed |
NCT01615731 -
Value of Mifepristone in Cervical Preparation Prior to Dilation and Evacuation 19-24 Weeks
|
N/A | |
| Completed |
NCT01597726 -
Cervical Priming Before Dilation & Evacuation
|
N/A | |
| Completed |
NCT02318212 -
Dilapan-S / Dilasoft E-Registry in Induced Abortion
|
N/A | |
| Terminated |
NCT00855842 -
Pilot Study of the Addition of Osmotic Dilators to Preparation Prior to Labor Induction Abortion
|
N/A | |
| Completed |
NCT00330993 -
Oral Mifepristone and Buccal Misoprostol Administered Simultaneously for Abortion Through 63 Days Gestation
|
Phase 2 | |
| Completed |
NCT00382538 -
Mifepristone and Mid-Trimester Termination of Pregnancy
|
N/A | |
| Completed |
NCT03080493 -
Gabapentin for Pain Control After Osmotic Dilator Insertion and Prior to D&E Procedure: a Randomized Controlled Trial
|
Phase 4 | |
| Completed |
NCT02485444 -
Oxytocin Infusion vs. Spontaneous Follow-up for Third-stage of Labor After Second-trimester Abortion
|
Phase 4 | |
| Completed |
NCT00969982 -
Mifepristone Plus Misoprostol Versus Misoprostol Alone for 2nd Trimester Abortion (14 - 21 Weeks Last Menstrual Period (LMP))
|
N/A | |
| Recruiting |
NCT02480543 -
Different Routes of Misoprostol Prior to First Trimester Surgical Abortion
|
Phase 4 | |
| Completed |
NCT00870272 -
Study of 400mcg Sublingual Versus 400mcg Buccal Misoprostol Following 200mg Mifepristone for Medical Abortion up to 63 Days Last Menstrual Period (LMP)
|
N/A | |
| Completed |
NCT02048098 -
Misoprostol for Second Trimester Termination of Pregnancy
|
Phase 3 |