Skip to main content
MedPathMedPath Home
Clinical Trials/ISRCTN06428555
ISRCTN06428555
Completed
Not Applicable

A prospective, randomised study to compare the effectiveness of the 24 hour versus 12 hour double doses regimen of levonorgestrel for emergency post-coital contraceptio

World Health Organisation (WHO) (Switzerland)0 sites2,071 target enrollmentApril 1, 2004
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsContraceptionPregnancy and Childbirth

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Contraception
Sponsor
World Health Organisation (WHO) (Switzerland)
Enrollment
2071
Status
Completed
Last Updated
11 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 1, 2004
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
World Health Organisation (WHO) (Switzerland)

Eligibility Criteria

Inclusion Criteria

  • •1\. Requesting emergency contraception within 120 hours of unprotected intercourse
  • •2\. Only one act of unprotected intercourse during current cycle
  • •3\. Willing to abstain from further acts during current cycle
  • •4\. Regular menstrual cycles (24 to 42 days)
  • •5\. Having at least one spontaneous cycle before current cycle
  • •6\. Available for follow\-up in the next six weeks
  • •7\. Negative pregnancy test
  • •8\. Willing to participate
  • •9\. Not breastfeeding
  • •10\. No use of hormonal contraceptives or of rhythm or natural family planning method of contraception during current cycle

Exclusion Criteria

  • •1\. Post\-abortion or post\-partum patients whose period had not yet returned
  • •2\. Regular use of prescription drugs before admission to the study
  • •3\. Intercourse during the treatment cycle greater than 120 hours before admission into the study

Outcomes

Primary Outcomes

Not specified

Similar Trials

Active, not recruiting
Phase 1
Comparison of the effect of autologous cell therapy with standard treatment in patients with diabetic foot
EUCTR2016-001397-15-CZInstitut klinické a experimentální medicíny40
Not yet recruiting
Phase 3
Comparison of efficacy of three types of laryngoscopes in adult patients posted for surgeryHealth Condition 1: K928- Other specified diseases of the digestive system
CTRI/2022/08/044684Department of Anaesthesiology and Critical Care Jawaharlal Nehru Medical College AMU Aligarh
Not yet recruiting
Phase 3
COMPARISON OF TWO DRUGS IN THE TREATMENT OF ORAL LICHEN PLANUSHealth Condition 1: L438- Other lichen planus
CTRI/2023/03/050453OT APPLICABLE
Completed
Phase 2
A study for comparing the effect of neutral and extended head positions in awake intubation using fibreoptic bronchoscope in adultsHealth Condition 1: 8- Other Procedures
CTRI/2023/06/053757-50
Not yet recruiting
Not Applicable
Comparison of two methods to decide amount of intravenous fluids to be given in open abdominal surgeries.Health Condition 1: C569- Malignant neoplasm of unspecifiedovary
CTRI/2018/12/016543Max Superspecilaity Hospital