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NCT06857461
Effect of the Uriclarity Program on Perceived Milk Supply in Postpartum Women in Piura-Peru
NA trial testing Uriclarity Program in Perceived Insufficient Milk Supply in 91 participants. Completed in 24 August 2025.
24 August 2025
Quick facts
| Lead sponsor | Crianzamor |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | prevention |
| Enrollment | 91 |
| Start date | 28 May 2025 |
| Primary completion | 24 August 2025 |
| Estimated completion | 24 August 2025 |
| Sites | 2 locations across Peru |
Drugs / interventions tested
- Uriclarity Program
Conditions studied
- Perceived Insufficient Milk Supply — all drugs for Perceived Insufficient Milk Supply →
Sponsor
Crianzamor
Who can join
18 and older, female only, with Perceived Insufficient Milk Supply. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this clinical trial is to assess whether the Uriclarity Program is effective in reducing the perception of insufficient milk supply (PIM) in postpartum women. The study also aims to evaluate the feasibility of implementing this program as a lactation support strategy. The main research questions are: Does the Uriclarity Program reduce the perception of insufficient milk supply among postpartum women? How does the program impact breastfeeding confidence and adherence to exclusive breastfeeding? Researchers will compare the Uriclarity Program to standard postpartum lactation counseling to determine its effectiveness. Participants will: Receive either the Uriclarity Program intervention or standard lactation counseling within 24-48 hours postpartum. Be evaluated on days 1, 3, 7, and 14 postpartum using the PIM questionnaire to assess changes in perception. Engage in follow-up via WhatsApp support groups (for the intervention group). This randomized controlled trial will provide evidence on whether the Uriclarity Program can effectively reduce maternal concerns about milk supply and support exclusive breastfeeding.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Uriclarity Program Reduces Perceived Insufficient Milk Supply in Early Postpartum: Randomized Controlled Trial
Vega JA, Rojas MY, Ashiyama JR. · · 2026 · DOI 10.21203/rs.3.rs-8634552/v1
Verify or expand the search:
- PubMed search for NCT06857461
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Perceived Insufficient Milk Supply
Currently open trials in the same condition.
- NCT07447609 — THE EFFECT OF REIKI ON BREASTFEEDING, PAIN AND COMFORT AFTER CESAREAN SECTION · NA · recruiting
Other Crianzamor trials
Trials by the same sponsor.
- NCT06751186 — Effect of Teté Dance on Breastfeeding Duration in Irritable Infants · NA · completed
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 NCT06857461 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Crianzamor
- Last refreshed: 8 September 2025
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/NCT06857461.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing