Obtaining LARCs immediately after delivery vs. 6-week follow-up visit by postpartum women - a medical record chart review
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- STATUS
- Not Recruiting
Summary
This research aims to conduct a retrospective medical record chart review to assess the population of patients who express a desire for long-acting reversible contraceptives (LARCs) in the immediate postpartum contraception in the form of DepoProvera, Nexplanon, and progestin intrauterine device (IUD). This study seeks to evaluate the clinical characteristics and demographics of women who requested for immediate postpartum contraception at the time of hospital admission but before delivery. Specifically, we aim to compare women who received contraception before being discharged from the hospital vs. waiting until their 6-week postpartum follow-up appointment. Additionally, we are interested in learning about the rate of fulfilled requests. We hypothesize that women who waited to receive contraception at their 6-week follow-up appointment as opposed to in-hospital, are more likely to have unfulfilled requests.
Description
This research aims to conduct a retrospective medical record chart review to assess the population of patients who express a desire for long-acting reversible contraceptives (LARCs) in the immediate postpartum contraception in the form of DepoProvera, Nexplanon, and progestin intrauterine device (IUD). This study seeks to evaluate the clinical characteristics and demographics of women who requested for immediate postpartum contraception at the time of hospital admission but before delivery. Specifically, we aim to compare women who received contraception before being discharged from the hospital vs. waiting until their 6-week postpartum follow-up appointment. Additionally, we are interested in learning about the rate of fulfilled requests. We hypothesize that women who waited to receive contraception at their 6-week follow-up appointment as opposed to in-hospital, are more likely to have unfulfilled requests.
Details
| Condition | healthy |
|---|---|
| Age | 100years or below |
| Clinical Study Identifier | TX8407 |
| Last Modified on | 19 February 2024 |
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