NCT06936436

Brief Summary

This study aims to evaluate whether the timing of postpartum Implanon insertion (immediately postpartum, early postpartum, or late postpartum) affects menstrual patterns

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
1mo left

Started May 2025

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress94%
May 2025Jun 2026

First Submitted

Initial submission to the registry

April 13, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 20, 2025

Completed
11 days until next milestone

Study Start

First participant enrolled

May 1, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Expected
Last Updated

April 23, 2025

Status Verified

April 1, 2025

Enrollment Period

1 year

First QC Date

April 13, 2025

Last Update Submit

April 18, 2025

Conditions

Outcome Measures

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.

    baseline

Interventions

implanon is a long acting ,reversible contraceptive implants used to prevent pregnancy

Eligibility Criteria

Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study 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

You may qualify if:

  • Postpartum women opting for Implanon as contraception.
  • No contraindications to hormonal contraception.

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (4)

  • Mazza D, Harrison C, Taft A, Brijnath B, Britt H, Hobbs M, Stewart K, Hussainy S. Current contraceptive management in Australian general practice: an analysis of BEACH data. Med J Aust. 2012 Jul 16;197(2):110-4. doi: 10.5694/mja11.11599.

    PMID: 22794058BACKGROUND
  • Richters J, Grulich AE, de Visser RO, Smith AM, Rissel CE. Sex in Australia: contraceptive practices among a representative sample of women. Aust N Z J Public Health. 2003;27(2):210-6. doi: 10.1111/j.1467-842x.2003.tb00810.x.

    PMID: 14696713BACKGROUND
  • . Product information: Implanon NXT, Schering-Plough Pty Ltd, 12 November 2010

    BACKGROUND
  • Product information: Implanon® Implant, Organon (Australia) Pty Ltd, 19 March 2008.

    BACKGROUND

MeSH Terms

Conditions

Menstruation Disturbances

Interventions

etonogestrel

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • AHMED MOHAMED ABBAS, PROF.DR

    Assiut University

    STUDY CHAIR
  • MOHAMED SAYED ABDELLAH, PROF.DR

    Assiut University

    STUDY CHAIR
  • ALAA AHMED MAKHLOUF, DR

    Assiut University

    STUDY CHAIR

Central Study Contacts

kholoud khalid KAMAL

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
OBSTETRICS AND GYNECOLOGY RESIDENT

Study Record Dates

First Submitted

April 13, 2025

First Posted

April 20, 2025

Study Start

May 1, 2025

Primary Completion

May 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

April 23, 2025

Record last verified: 2025-04