The Biofeedback Therapy in Solitery Rectal Ulser Patients BIOFEEDBACK

Clinical Trial Description

dyssynergia treating ulcers caused by treatment with biofeedback ;

Study Design

Observational Model: Case-Crossover, Time Perspective: Prospective

Related Conditions & MeSH terms

Rectal Ulcer

See also
	Status	Clinical Trial	Phase
	Not yet recruiting	`NCT05912712` - Autologous Platelet-rich Plasma (PRP) and Thrombin Coagulum for the Topical Treatment of Rectal Mucosal Ulcers	Phase 1

See also

Status

Clinical Trial

Phase

Not yet recruiting

NCT05912712 - Autologous Platelet-rich Plasma (PRP) and Thrombin Coagulum for the Topical Treatment of Rectal Mucosal Ulcers

Phase 1

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	NCT02334995
Study type	Observational
Source	Ege University
Contact	Serhat Bor
Phone	+902323905216
Email	serhatbor@yahoo.com
Status	Recruiting
Phase	N/A
Start date	January 2014
Completion date	January 2017

The Biofeedback Therapy in Solitery Rectal Ulser Patients BIOFEEDBACK THERAPY

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms