Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07331168
Brief 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.
Study:
NCT07331168
Study Brief:
Protocol Section:
NCT07331168