Trial · NCT03585504
Immediate Versus Delayed Insertion of Implanon in Postpartum Adolescents
NCT03585504, Phase 3, Completed, Medical University of South Carolina; results first posted 2018-10-04
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Immediate Versus Delayed Insertion of Implanon in Postpartum Adolescents. Trials, record NCT03585504. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03585504
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Immediate Versus Delayed Insertion of Implanon in Postpartum Adolescents
- NCT number
- NCT03585504
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 81 participants, actual
- Lead sponsor
- Medical University of South Carolina
- Conditions
- Contraceptive Usage
- Interventions
- Etonogestrel contraceptive implant
- First posted
- 2018-07-13
- Last updated
- 2018-10-04
- Results first posted
- 2018-10-04
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of Participants With Contraceptive Implant Continuation at Six Months Postpartum | 6 months | We compare the number of participants continuing the implant at six months in each group. |
| Secondary | Number of Participants That Reported They Were Somewhat or Very Satisfied With Their Subjective Bleeding Experience at Six Months Postpartum. | 6 months | Compare the number of participants who reported that they were somewhat or very satisfied with their subjective bleeding experience at six months postpartum in each group. Each participant was asked, "Please indicate your overall level of satisfaction with your bleeding." The response options were "very satisfied", "somewhat satisfied", "somewhat dissatisfied", and "very dissatisfied". The outcome measure was treated as a categorical variable. |
| Secondary | Number of Participants Who Reported That They Were Somewhat or Very Satisfied With the Contraceptive Implant at Six Months Postpartum. | 6 months | Comparison of the number of participants in each group who report that they were somewhat or very satisfied with their contraceptive method choice at six months postpartum in each group. Participants were asked, " How would you rate your overall satisfaction with implanon?" The response options were "very satisfied", "somewhat satisfied", "somewhat dissatisfied", and "very dissatisfied". The outcome measure was treated as a categorical variable. |
Source ClinicalTrials.gov
Outcomes3
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Participants With Contraceptive Implant Continuation at Six Months Postpartum | 6 months | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Participants That Reported They Were Somewhat or Very Satisfied With Their Subjective Bleeding Experience at Six Months Postpartum. | 6 months | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Participants Who Reported That They Were Somewhat or Very Satisfied With the Contraceptive Implant at Six Months Postpartum. | 6 months | Participants | COUNT_OF_PARTICIPANTS |
Source ClinicalTrials.gov
Results by group6
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Participants With Contraceptive Implant Continuation at Six Months Postpartum | Intervention Group | 15 | Participants | ||
| Number of Participants With Contraceptive Implant Continuation at Six Months Postpartum | Control Group | 7 | Participants | ||
| Number of Participants That Reported They Were Somewhat or Very Satisfied With Their Subjective Bleeding Experience at Six Months Postpartum. | Intervention Group | 10 | Participants | ||
| Number of Participants That Reported They Were Somewhat or Very Satisfied With Their Subjective Bleeding Experience at Six Months Postpartum. | Control Group | 8 | Participants | ||
| Number of Participants Who Reported That They Were Somewhat or Very Satisfied With the Contraceptive Implant at Six Months Postpartum. | Intervention Group | 14 | Participants | ||
| Number of Participants Who Reported That They Were Somewhat or Very Satisfied With the Contraceptive Implant at Six Months Postpartum. | Control Group | 6 | Participants |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Intervention Group | 41 | |
| Overall Study | STARTED | Control Group | 40 | |
| Overall Study | COMPLETED | Intervention Group | 15 | |
| Overall Study | COMPLETED | Control Group | 11 | |
| Overall Study | NOT COMPLETED | Intervention Group | 26 | |
| Overall Study | NOT COMPLETED | Control Group | 29 |
Source ClinicalTrials.gov
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Intervention Group | 0 | 15 |
| Total, all-cause mortality | Control Group | 0 | 11 |
| Total, other adverse events | Intervention Group | 0 | 15 |
| Total, other adverse events | Control Group | 0 | 11 |
| Total, serious adverse events | Intervention Group | 0 | 15 |
| Total, serious adverse events | Control Group | 0 | 11 |
Source ClinicalTrials.gov
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 36302159 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons5
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Intervention Group vs Control Group: Number of Participants With Contraceptive Implant Continuation at Six Months Postpartum | Trial comparisons |
| Intervention Group vs Control Group: Number of Participants Who Reported That They Were Somewhat or Very Satisfied With the Contraceptive Implant at Six Months Postpartum. | Trial comparisons |
| Intervention Group vs Control Group: deaths from any cause | Trial comparisons |
| Intervention Group vs Control Group: Number of Participants That Reported They Were Somewhat or Very Satisfied With Their Subjective Bleeding Experience at Six Months Postpartum. | Trial comparisons |
| Intervention Group vs Control Group: serious adverse events | Trial comparisons |
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03585504
GET https://conductscience.org/api/trials/v1/NCT03585504/registered