Hysteroscopic Evaluation of Cesarean Scar Defect

See also
Status	Clinical Trial	Phase
Completed	`NCT04073264` - Isthmocele After Two Different Sutures in Cesarean Section	N/A
Completed	`NCT02717312` - Prevalence, Risk Factors and Consequences Related to Cesarean Scar Defect (Defect in Cesarean Scar)
Recruiting	`NCT05276518` - Double Vers Single in Cesarean Incision

See also

Status

Clinical Trial

Phase

Completed

NCT04073264 - Isthmocele After Two Different Sutures in Cesarean Section

N/A

Completed

NCT02717312 - Prevalence, Risk Factors and Consequences Related to Cesarean Scar Defect (Defect in Cesarean Scar)

Recruiting

NCT05276518 - Double Vers Single in Cesarean Incision

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	NCT03780699
Study type	Observational
Source	Ain Shams University
Contact	Radwa R Ali, MD
Phone	01283492979
Email	radwaebed@yahoo.com
Status	Recruiting
Phase
Start date	April 1, 2018
Completion date	September 1, 2019

Hysteroscopic Evaluation of Cesarean Scar Defect

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms