Other Clinical Trial - Effects of Abdominal Binders & TENS on Puerperium

See also
Status	Clinical Trial	Phase
Completed	`NCT03136159` - The Role of Antimicrobial Foam Dressing in Prevention of Cesarean Section Wound Complications	N/A
Not yet recruiting	`NCT05187728` - Association Between the Adenomyosis and the Clinical Outcomes of Vaginal Repair of CesareanSectionScar Defects
Recruiting	`NCT03644433` - Impact of Uterine Closure Techniques on the Cesarean Scar Thickness After Repeated Cesarean Section	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT03136159 - The Role of Antimicrobial Foam Dressing in Prevention of Cesarean Section Wound Complications

N/A

Not yet recruiting

NCT05187728 - Association Between the Adenomyosis and the Clinical Outcomes of Vaginal Repair of CesareanSectionScar Defects

Recruiting

NCT03644433 - Impact of Uterine Closure Techniques on the Cesarean Scar Thickness After Repeated Cesarean Section

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT06303245
Study type	Interventional
Source	Riphah International University
Contact	imran amjad
Phone	03324390125
Email	imran.amjad@riphah.edu.pk
Status	Recruiting
Phase	N/A
Start date	February 23, 2023
Completion date	September 1, 2024

Effects of Abdominal Binders and TENS on Puerperium Period After Cesarean Section

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms