Viewing Study NCT06413186



Ignite Creation Date: 2024-05-19 @ 5:33 PM
Last Modification Date: 2024-10-26 @ 3:29 PM
Study NCT ID: NCT06413186
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-05-14
First Post: 2024-04-25

Brief Title: Effect of Placenta Delivery Method on Pain Bleeding and Comfort
Sponsor: Tarsus University
Organization: Tarsus University

Study Overview

Official Title: Examining the Effect of Placenta Delivery Method on Postpartum Pain Bleeding and Comfort of Women Randomized Controlled Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this thesis is to examine the effect of the placenta delivery method on womens postpartum pain bleeding and comfort It is a randomized controlled experimental study The research will be conducted at Mersin Tarsus state hospital between March 2024 and August 2024 The study will be conducted with 140 primiparous women 70 primiparous pregnant women in the experimental group and 70 primiparous pregnant women in the control group who meet the research criteria and apply to the delivery room of Tarsus State Hospital between these dates The research will be carried out with a control group those receiving routine hospital protocolwhere the placenta is delivered with controlled cord traction and an experimental group physiological separation of the placenta with a mixed method Interventions applied to research groups vary depending on the characteristics of the group In both groups interventions in the delivery room will be performed by the researcher midwife If any complications develop during the research independent of the interventions if the woman undergoes a cesarean section or if situations that meet the exclusion criteria occur that woman will be excluded from the sample The researcher will apply a routine hospital birth management protocol to both groups during the first three stages of labor However the way the placenta is delivered in the third stage physiological with mixed management or controlled cord traction with active management will differ The researcher will apply the Visual Analogue Scale VAS twice at the beginning and at the end of the third phase of labor apply the Postpartum Comfort Scale at the 4th postpartum hour and record hemoglobin and hematocrit values at admission to the hospital which is the hospitals routine protocol and in the hemogram test at the 6th hour postpartum HB and HCT values will be used to interpret the amount of postpartum bleeding The hypotheses of the research are as follows H1 In the active management of the 3rd stage of labor delivery of the placenta with controlled cord traction affects the womans perception of postpartum pain

H2 In the active management of the 3rd stage of labor delivering the placenta with controlled cord traction affects the womans amount of postpartum bleeding

H3 In the active management of the 3rd stage of labor delivering the placenta with controlled cord traction affects the womans postpartum comfort level

H4 In the mixed management of the 3rd stage of labor physiological delivery of the placenta affects the womans perception of postpartum pain

H5 In the mixed management of the 3rd stage of labor physiological delivery of the placenta affects the amount of postpartum bleeding of the woman

H6 In the mixed management of the 3rd stage of labor physiological delivery of the placenta affects the womans postpartum comfort level
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None