the Effect of Implanon on Menstrual Patterns
ConditionMenstrual Irregularities
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
AgeNot listed
SponsorAssiut University
About this trial
This study aims to evaluate whether the timing of postpartum Implanon insertion (immediately postpartum, early postpartum, or late postpartum) affects menstrual patterns
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Postpartum women opting for Implanon as contraception.
No contraindications to hormonal contraception.
Disqualifiers
. Women with known bleeding disorders.
Use of other hormonal contraceptives during the study period.
Postpartum complications such as severe infections or retained products of conception
Trial population
Women will be grouped into: 1. Immediate postpartum (Insertion within 48 hours of delivery). 2. Early postpartum (Insertion between 4-6 weeks postpartum). 3. Late postpartum (Insertion after 6 weeks postpartum
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Implanon (Etonogestrel)
Other interventionimplanon is a long acting ,reversible contraceptive implants used to prevent pregnancy
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
The Effect of Implanon on Menstrual Patterns According to Timing of Insertion After Delivery
To compare the effect of Implanon insertion at different postpartum intervals (immediate, early, late) on menstrual cycle patterns * To assess the prevalence of irregular bleeding, amenorrhea, and prolonged bleeding across different insertion groups. * To analyze general trends in menstrual changes, regardless of insertion timing.
Time frame
baselineLocations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: