Viewing Study NCT06168630



Ignite Creation Date: 2024-05-06 @ 7:52 PM
Last Modification Date: 2024-10-26 @ 3:15 PM
Study NCT ID: NCT06168630
Status: RECRUITING
Last Update Posted: 2023-12-13
First Post: 2023-12-04

Brief Title: Effects of Manual Lymph Drainage on Breast Engorgement in Postpartum Period
Sponsor: Riphah International University
Organization: Riphah International University

Study Overview

Official Title: Effects of Manual Lymph Drainage on Breast Engorgement Pain and Self Efficacy in Postpartum Period
Status: RECRUITING
Status Verified Date: 2023-12
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: There have been many studies on the treatment of breast engorgement there is a lack of research comparing the effectiveness of manual lymph drainage with massage Therefore this study will be a randomized controlled trial that aims to compare the effects of manual lymph drainage with massage on breast engorgement pain and self efficacy in the postpartum period
Detailed Description: The study will be a randomized controlled trial and will be conducted in Jinnah hospital Lahore This study will be completed in time duration of 10 months after the approval of synopsis Non probability convenience sampling technique will be used and 35 participants will be recruited in study after randomization The subjects will be divided into two groups and the group A will receive manual lymph drainage and group B will receive massage whereas cold pack will be used as a baseline treatment The tools that will be used for pre and post treatment assessment are NPRS 6 point self rated engorgement scale and breast feeding self efficacy questionnaire The data will be assessed after 5 days of treatment using 2 tailed t test After data collection data will be analyzed by using SPSS version 25

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