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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 49
Healthy Volunteers: t
View:

• Over 18 years of age

• Primiparous, singleton pregnancy

• Gestational age \>37 weeks, elective cesarean section under spinal anesthesia

• No issues with breastfeeding the baby or herself during the postpartum period

• Voluntarily participating

Locations
Other Locations
Turkey
Kütahya Health Sciences University
RECRUITING
Kütahya
Contact Information
Primary
Havva Yeşildere Sağlam, PhD
havva.yesilderesaglam@ksbu.edu.tr
0 (274) 260 00 43
Time Frame
Start Date: 2025-10-01
Estimated Completion Date: 2026-01-31
Participants
Target number of participants: 68
Treatments
Experimental: Intervention
Active warming group
No_intervention: Control
Control group
Related Therapeutic Areas
Sponsors
Collaborators: Bilecik Seyh Edebali Universitesi, Kutahya City Hospital
Leads: Kutahya Health Sciences University

This content was sourced from clinicaltrials.gov