Rectal Sensory Training - A Study of Two Techniques

NCT ID: NCT00982839

Last Updated: 2014-09-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 70 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-03-31
• Study Completion Date: 2014-07-31

Brief Summary

At least 60% of patients with constipation and dyssynergic defecation (anismus) and between 30-50% of patients with fecal incontinence exhibit impaired rectal sensation. The problem may be improved by biofeedback therapy. Traditionally, biofeedback therapy was performed by using a syringe-assisted technique. Although some respond to this method, many, particularly those with severe rectal hyposensitivity have proved to be refractory. Also, repeated inflation and deflation of a large volume of air, using a hand-held syringe is cumbersome and time consuming. Recently, in pilot observations, the investigators have seen that a barostat-assisted technique of biofeedback therapy was simpler and easier to perform and could possibly be more effective. The investigators' aims are:

1. To perform a randomized controlled study that compares the syringe-assisted sensory conditioning (biofeedback therapy) technique with the barostat assisted sensory conditioning for improving the rectal sensation in patients with rectal hyposensitivity and bowel dysfunction.

2. To investigate the impact of sensory conditioning on psychosocial issues and quality of life.

3. To compare the cost-effectiveness of each therapeutic modality The specific hypotheses that will be tested are;

When compared to those who receive syringe-assisted training, patients receiving barostat training will demonstrate:

1. Lower sensory thresholds for rectal perception (first sensation, desire to defecate and urgency)

2. Greater satisfaction with bowel function (VAS Score), stool frequency,consistency & straining.

3. Better learning ability and greater ease of administering this training.

Conditions

Rectal Hyposensitivity; Constipation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Syringe Conditioning

A syringe will be used to inflate the balloon at the end of the probe which is inside of the rectum.

Group Type: ACTIVE_COMPARATOR

Syringe Conditioning

Intervention Type: PROCEDURE

A syringe will be used to inflate the balloon at the end of the probe which is inside of the rectum.

Barostat Conditioning

A barostat machine will be used to inflate the balloon at the end of the probe which is inside of the rectum.

Group Type: EXPERIMENTAL

Barostat Conditioning

Intervention Type: PROCEDURE

A barostat machine will be used to inflate the balloon at the end of the probe which is inside of the rectum.

Interventions

Syringe Conditioning

A syringe will be used to inflate the balloon at the end of the probe which is inside of the rectum.

Intervention Type: PROCEDURE

Barostat Conditioning

A barostat machine will be used to inflate the balloon at the end of the probe which is inside of the rectum.

Intervention Type: PROCEDURE

Other Intervention Names

Syringe; Barostat

Eligibility Criteria

Inclusion Criteria

• Patients categorized as having dyssynergic defecation or slow transit constipation or normal transit constipation will be eligible.
• All patients must demonstrate rectal hyposensitivity during a manometry with values that are outside 2 S.D. of normal range and demonstrate any two of the following: a) Threshold for 1st sensation > 40 cc. b) Threshold for desire to defecate > 130 cc. c) Threshold for urgency to defecate >180 cc.

Exclusion Criteria

• Patients taking drugs that are constipating, (e.g.; calcium channel antagonists will either be excluded or drug discontinued).
• Patients with co-morbid illnesses; severe cardiac disease, chronic renal failure or previous gastrointestinal surgery except cholecystectomy and appendectomy.
• Neurologic diseases e.g.; head injury, epilepsy, multiple sclerosis, strokes, spinal cord injuries.
• Impaired cognizance (mini mental score of < 15) and/or legally blind.
• Pregnant or likely to conceive during the course of the study. Women with potential for pregnancy must be willing to use contraceptive measures during the study. Urinary pregnancy tests will be performed on such women prior to any radiologic procedures.
• Hirschsprung's disease.
• Alternating constipation and diarrhea (22).
• Ulcerative/Crohns colitis.
• Previous pelvic surgery, rectocele/bladder repair, radical hysterectomy, anal surgery.
• Rectal prolapse or anal fissure. 11) Patients with severe rectal hyposensitivity, first sensation or desire to defecate > 320 cc

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Augusta University

OTHER

Sponsor Role: lead

Responsible Party

Satish Rao

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Satish Rao, Md, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Iowa

Locations

University of Iowa Hospitals and Clinics

Iowa City, Iowa, United States

Countries

United States

Other Identifiers

5R01DK057100-08

Identifier Type: NIH

Identifier Source: org_study_id

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