Sohag university Hospital
Sohag, Egypt
Location status: Recruiting
Location contact
magdy m amin, professor
CONTACT
NCT Number: NCT06564064
The effect of abdominal binders on patient's wellbeing after cesarean delivery
Interested in participating?
Request InfoFemale
Interventional
Not applicable
Sohag, Egypt
Location status: Recruiting
magdy m amin, professor
CONTACT
The effect of abdominal binders on patient's wellbeing after cesarean delivery 12 hours and one week after cesarean section
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
any female post cesarean section of singleton 34 wks gestaion fetus with previous cs
Exclusion criteria
primary cs any hypertensive disorder with pregnancy any neurologiacal disease general anasthesia or vertical incision
study group will be abdominal binders and control group will be control group , 12 hrs and one week later VAS and QOR 40 will assess patient,s wellbeing
Time frame: 6 months
abdominal binders will be fit on patient abdomin 2 hrs post cs and VAS will be assessed 12 hrs post cesarean section
Time frame: one week postoperatively
effect after one week on quality of recovery ( infection, hematoma, seroma) by QOR 40
Contact information is provided by the study sponsor or research team.
abdou s aitallah, professor
CONTACT
esraa s abd ellatif, resident
CONTACT
Sohag University
Other
The Effect of Abdominal Binders on Patient's Wellbeing After Cesarean Delivery :a Prospective Comparative Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07403929
Chronic Pain, Fibromyalgia
Istanbul, Turkey (Türkiye)
View Trial DetailsNCT06791044
Atrophy, Bone Diseases
Nea Liosia, Athens, Greece
View Trial DetailsNCT07738718
Dental Anxiety, Neurologic Manifestations
Ar Rass, Al-Qassim Region, Saudi Arabia
View Trial DetailsNCT05563792
Agnosia, Chronic Pain
Indianapolis, Indiana, United States
View Trial Details