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NCT06682871
Breastfeeding Evaluation of Puerperal Women Who Had Cesarean Delivery in Our Hospital
NA trial testing Analgesia in Breast Feeding in 75 participants. Completed in 25 July 2025.
23 July 2025
Quick facts
| Lead sponsor | Konya City Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | quadruple |
| Primary purpose | prevention |
| Enrollment | 75 |
| Start date | 1 January 2024 |
| Primary completion | 23 July 2025 |
| Estimated completion | 25 July 2025 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Analgesia — full drug profile →
Conditions studied
- Breast Feeding — all drugs for Breast Feeding →
- Analgesia — all drugs for Analgesia →
Sponsor
Konya City Hospital
Who can join
Adults 18 to 45, any sex, with Breast Feeding or Analgesia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
İntroduction The World Health Organisation (WHO) and United Nations Children's Fund (UNICEF) recommends that infants are exclusively breastfed for a minimum of 6 months, with continued breastfeeding recommended until child age of 2 years or over to optimize growth, development, and health. Breast milk shows significant benefits for the physical and mental health of mothers and infants, including the promotion of maternal and infant bonding, the reduction of neonatal mortality, the reduction of maternal postoperative complications, and the development of newborns. Breastfeeding has been associated with improved maternal/infant bonding and increased child intelligence. It is also clear that medical interventions during labor and birth, including a caesarean section, impact on women's infant feeding decisions and are a cause for concern given increasing global caesarean birth rates, with woman who have a planned caesarean birth reported as less likely to intend to breastfeed than women who did not have a planned caesarean birth or had a vaginal birth. Infrequent feeding and women's limited mobility in the early days following surgery may impede efforts to provide basic infant care. High levels of postoperative pain, particularly in the first 24 hrs, were also found to have a negative impact on women's breastfeeding experiences. Cesarean delivery is linked with lower rates of early breastfeeding initiation. Pain management after casarean delivery remains challenging. The best-accepted traditional analgesic approach is continuous epidural analgesia. However, epidural analgesia is rapidly being replaced by transversus abdominis plane (TAP) blocks. TAP infiltration is an alternative to epidural blocks for providing postoperative analgesia to the anterior abdominal wall. TAP infiltrations are relatively easy to perform, generally safe, and can be performed in patients who are anti-coagulated. TAP infiltration can be performed as a single injection, or a catheter can be inserted for continuous local anesthetic infusion.
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 NCT06682871
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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Related trials
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Trials testing the same drug.
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Other recruiting trials for Breast Feeding
Currently open trials in the same condition.
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- 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 Konya City Hospital trials
Trials by the same sponsor.
- NCT07504705 — Comparison of Intertransverse Process and Erector Spinae Plane Blocks in Acute Postoperative Analgesia Management for La · NA · not yet recruiting
- NCT07525167 — Early Prediction of Bronchopulmonary Dysplasia in Preterm Infants Using Clinical Data · not yet recruiting
- NCT07335250 — Intertransverse Process Block for Postoperative Analgesia After Thoracotomy and Lobectomy · NA · recruiting
- NCT07511985 — Effect of Rebound Pain on Chronic Postsurgical Pain After Total Knee Arthroplasty · not yet recruiting
- NCT07295158 — Effect of Sevoflurane vs Desflurane on Mechanical Power in Laparoscopic Cholecystectomy · NA · 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 NCT06682871 (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 Konya City Hospital
- Last refreshed: 3 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/NCT06682871.
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