Induced Abortion Clinical Trial
Official title:
Is Oxytocin Given During Surgical Procedure for Abortion Before 12 Weeks of Pregnancy Useful ?
This is a randomized, single-blind study using oxytocin 5U i.v. during surgical abortion in one arm of the study, and no medication in the other arm of the study. Comparison is done between the two groups measuring the following outcomes: pain, nausea and blood loss. The investigators' hypothesis is that there will be no significant differences between the two groups.
All women seeking surgical abortion before 12 weeks of pregnancy will be invited to participate in the study. We will include 400 patients. Written consent is given. Pain is measured on a VAS-scale (1-10) 2 hours post operatively and repeated 2 days postoperatively. Nausea is categorized in 4 groups, from 1 (no nausea) to 4 (pronounced nausea with vomiting)and is registered together with bloodloss also during the hospital stay (2 hours) and 2 days postoperatively. The two groups will be compared. ;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Not yet recruiting |
NCT02208596 -
The Feasibility of Different Doses of Etomidate Admixed With Propofol in Induced Abortion: A Randomized, Double Blind Controlled Trial
|
Phase 4 | |
| Completed |
NCT02412618 -
Same-Day Mifepristone-Misoprostol Compared to Misoprostol Only for Surgical Abortion Cervical Preparation
|
Phase 4 | |
| Completed |
NCT01842100 -
To Compare the Strategies of Universal Antibiotic Prophylaxis Versus Screen-and-treat in Reducing Infective Complications and Re-infection in Women Who Undergo Termination of Pregnancy
|
N/A | |
| Completed |
NCT03727308 -
Study of Clinic-based Versus Self-use of Medical Abortion Pills
|
||
| Completed |
NCT00482209 -
Study of 400mcg Versus 800mcg Buccal Misoprostol Following Mifepristone 200mg for Abortion up to 63 Days Gestation
|
N/A | |
| Recruiting |
NCT04242212 -
Study of Clinic-based vs. Self-use of a Misoprostol-only Regimen for Induced Abortion
|
||
| Completed |
NCT00621543 -
Insertion of an Intrauterine Device (IUD) After Medical Abortion
|
N/A | |
| Recruiting |
NCT01636063 -
Mifepristone Versus Misoprostol for Cervical Preparation Prior to Surgical Abortion Between 11 to 15 Weeks
|
N/A | |
| Completed |
NCT01173003 -
Expansion Study of a Simplified Regimen of Medical Abortion Thru 63 Last Menstrual Period (LMP) in Tunisia
|
N/A | |
| Completed |
NCT05532085 -
Assessment of Pain During an Abortion With Knowledge of the Predictive Factors of Pain.
|
||
| Terminated |
NCT01776957 -
Post Abortion IUD & Recurrent Abortion 2005-2006
|
||
| Completed |
NCT01047748 -
A Trial of Digoxin Before Second-Trimester Abortion
|
N/A | |
| Completed |
NCT00401440 -
Comparison of Two Regimens of Misoprostol for Second Trimester Medical Termination of Pregnancy
|
Phase 4 | |
| Completed |
NCT00619658 -
The Feasibility of Simplified Telephone Follow-up After Medical Abortion
|
N/A | |
| Completed |
NCT00324519 -
Randomized Trial Comparing Misoprostol and Foley Bulb for Pregnancy Termination in the Second Trimester
|
Phase 4 | |
| Completed |
NCT04181541 -
Midlevel Versus Physician-provided Medical Abortion in the Second Trimester
|
N/A | |
| Completed |
NCT00286208 -
Study of Sublingual Versus Oral Misoprostol Administration Following Mifepristone 200 mg for Abortion up to 63 Days Gestation
|
N/A | |
| Completed |
NCT01085825 -
Study of the Sensitivity of Manual vs Electric Aspiration to Detect Completed Early Abortion
|
N/A |