Last reviewed · How we verify
NCT03568851
Reproductive Health Outcomes by Method of Breast Milk Feeding
trial in Breast Feeding in 394 participants. Completed in 14 January 2021.
14 January 2021
Quick facts
| Lead sponsor | University of California, Davis |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 394 |
| Start date | 27 June 2018 |
| Primary completion | 14 January 2021 |
| Estimated completion | 14 January 2021 |
| Sites | 1 location across United States |
Conditions studied
- Breast Feeding — all drugs for Breast Feeding →
- Milk Expression, Breast — all drugs for Milk Expression, Breast →
- Amenorrhea, Postpartum — all drugs for Amenorrhea, Postpartum →
Sponsor
University of California, Davis
Who can join
Adults 15 to 45, female only, with Breast Feeding or Milk Expression, Breast. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this research is to determine whether there are differences in ovarian suppression between women who are feeding at the breast compared with women who are pumping. * In the main study, the aim is to compare reproductive health outcomes, including amenorrhea rates, duration of lactation, and resumption of sexual activity, between mothers who are exclusively breastfeeding (i.e. feeding at the breast) and those who are pumping after a term or preterm delivery. * In the sub-study, the aim is to determine the feasibility and acceptability of using urinary luteinizing hormone (LH) detection kits at home to detect ovulation in exclusively breastmilk feeding women.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT03568851
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Breast Feeding
Currently open trials in the same condition.
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- NCT07281339 — Effect of Hypnobreastfeeding Education in High-Risk Pregnant Women · NA · recruiting
- NCT06621238 — The Effect of Musıc on Labor Paın, Anxıety and Breastfeedıng Success · NA · recruiting
- NCT06691932 — At-the-Breast vs. Expressed Human Milk: Genesis of Infant Nutrition (BEGIN) · recruiting
Other University of California, Davis trials
Trials by the same sponsor.
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- NCT07322133 — Dopamine vs. Norepinephrine for Hypotension in Neonates With Pulmonary Hypertension (DONE) · Phase 4 · recruiting
- NCT07384767 — Efficacy and Safety of Topical Timolol in Secondary Intention Surgical Wounds Healing · Phase 2 · not yet recruiting
- NCT07267494 — Image-Guided Herniorrhaphy Study · NA · not yet recruiting
- NCT04614714 — Milk Volume Outcomes Following Oral Nicotinamide Riboside Supplementation in Mothers of Extremely Preterm Infants · Phase 2, PHASE3 · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03568851 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of California, Davis
- Last refreshed: 18 August 2021
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03568851.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing