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Study identifier: NCT07331168 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

EVALUATION OF THE EFFECT OF ACTIVE WARMING APPLIED TO THE MOTHER DURING CESAREAN SECTION ON POST-BREASTFEEDING OUTCOMES: A RANDOMIZED CONTROLLED STUDY

Condition: Cesarean Resection · Breastfeeding · Thermal Comfort  ·  Sponsor: Kutahya Health Sciences University

PhaseNA
Planned participants68
Who can joinFemale, 18 Years to 49 Years
Healthy volunteersYes

About this study

Hypothermia is a complication of cesarean section and a cause of breastfeeding problems. Preventing maternal hypothermia is one of the goals of the enhanced postoperative recovery (ERAS) protocol and is important for the health of both mother and baby. This clinical trial aims to determine the effects of active warming during and after cesarean delivery on breastfeeding outcomes, thermal comfort, and perceived insufficient milk supply. The primary questions it aims to answer are: 1. To evaluate the effect of active warming during cesarean delivery on mothers' perception of thermal comfort. 2. To evaluate the effect of active warming after cesarean delivery on mothers' perceived insufficient milk supply. 3. To determine the effect of active warming after cesarean delivery on breastfeeding success. Participants: Warming will be provided using an active warming bed during cesarean delivery (45 minutes). Warming will continue in the postpartum care unit (45 minutes). The control group will not receive any warming and will receive the hospital's standard care procedure.

This description comes directly from the study's public registry record.

Talk to the study team

Havva Yeşildere Sağlam, PhD  ·  0 (274) 260 00 43  ·  havva.yesilderesaglam@ksbu.edu.tr

Always discuss trial participation with your own doctor first.

Locations (1)

Kütahya Health Sciences UniversityKütahya, None Selected, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07331168