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Keep Contraceptive Arm Long Acting-iMplant (CALM) and Carry On

NCT04725643 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 55

Last updated 2024-01-23

No results posted yet for this study

Summary

The investigators will conduct an observational study comparing the number of bleeding days before and after contraceptive implant (Nexplanon) replacement.

Conditions

  • Contraception
  • Contraceptive Usage
  • Family Planning

Interventions

DEVICE

Track bleeding patterns before and after implant

Participants will report if they had bleeding and the amount based on the Pictorial Blood Assessment Chart. Participants will also complete weekly surveys regarding their satisfaction with their bleeding. We will also ask participants to complete a survey regarding their satisfaction with their bleeding at end of month 2 and at the end of month 3 after replacement of their contraceptive implant.

Sponsors & Collaborators

Principal Investigators

  • Sheila Mody, MD, MPH · University of California, San Diego

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-02-17
Primary Completion
2024-01-11
Completion
2024-12-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04725643 on ClinicalTrials.gov