Enema Use and Acceptability in HIV Negative Men Who Have Sex With Men
This study has been completed.
Sponsor:
Johns Hopkins University
Collaborator:
University of California, Los Angeles
Information provided by:
Johns Hopkins University
ClinicalTrials.gov Identifier:
NCT00696618
First received: June 4, 2008
Last updated: August 3, 2009
Last verified: August 2009
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Purpose
This study is looking at 3 different types of enemas used before receptive anal intercourse in men who have sex with men (MSM). We are investigating whether the enemas cause any damage to the lining of the colon, how far up the colon the enemas travel after they are given, and how much study participants like using each of the enemas.
| Condition | Intervention |
|---|---|
|
HIV Infections |
Drug: Fleets enema Drug: tap water enema Drug: Normosol-R enema |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Single Group Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Prevention |
| Official Title: | A Randomized, Blinded, Comparative Study of the Mucosal Toxicity, Colorectal Distribution, and Participant Acceptability of Three Different Preparatory Enemas (Hypo-, Iso-, and Hyper-osmolar) |
Resource links provided by NLM:
Genetics Home Reference related topics:
complement factor I deficiency
MedlinePlus related topics:
HIV/AIDS
U.S. FDA Resources
Further study details as provided by Johns Hopkins University:
Primary Outcome Measures:
- To evaluate the mucosal toxicity of enemas of varying osmolality [ Time Frame: One year ] [ Designated as safety issue: Yes ]
| Enrollment: | 9 |
| Study Start Date: | July 2007 |
| Study Completion Date: | July 2009 |
| Primary Completion Date: | July 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: A |
Drug: Fleets enema
hyper-osmolar preparation
|
| Experimental: B |
Drug: tap water enema
hypo-osmolar preparation
|
| Experimental: C |
Drug: Normosol-R enema
iso-osmolar preparation
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Male
- ≥ Age of 18
- HIV-1 status antibody negative as documented at screening
A history of RAI at least twice per month in the prior 3 months*
- Required to assure that subjects are likely to complete each stage of enema test article use in a reasonable amount of time.
- History of enema use prior to RAI at least some of the time
- Willing to use each study product prior to RAI on 3 separate occasions.
- Willing to refrain from RAI for 48 hours before and after inpatient periods.
- Willing to use condoms for the duration of the study
- Availability to return for all study visits, barring unforeseen circumstances
- Understands and agrees to local STI reporting requirements
- Able and willing to communicate in English
- Able and willing to provide written informed consent to take part in the study
- Able and willing to provide adequate information for locator purposes
Exclusion Criteria:
- Female
- HIV positive at baseline
- History of inflammatory bowel disease
- Active inflammatory condition of the GI tract at baseline
- Active rectal infection at Visit 2 (Infections identified during the screening period must be treated prior to Visit 2)
- Presence of any painful anorectal conditions that would be tender to manipulation. (Participants with hemorrhoids and/or anal warts that are not painful may participate.)
- History of prosthetic cardiac valves, including bioprosthetic and homograft valves, previous bacterial endocarditis, surgically constructed systemic pulmonary shunts or conduits, and complex cyanotic congenital heart disease such as single ventricle states, transposition of the great arteries, tetralogy of Fallot or similar conditions that put the subject at high risk for bacteremia during endoscopy, hence requiring antibiotic prophylaxis.
- Unwillingness to refrain from chronic use of aspirin and NSAIDs.
- Use of warfarin or heparin
- Use of systemic immunomodulatory medications within 72 hours of Visit 2 baseline
- Use of rectally administered medications, including over-the-counter enemas, within 72 hours of Visit 2 baseline
- Use of product containing nonoxyl-9 rectally within 72 hours of Visit 2
- Use of any investigational products within 72 hours of Visit 2 baseline
- Any other clinical condition or prior therapy that, in the opinion of the investigator, would make the patient unsuitable for the study or unable to comply with the study requirements. Such conditions may include, but are not limited to, current or recent history of severe, progressive, or uncontrolled renal, hepatic, hematological, gastrointestinal, endocrine, pulmonary, neurological, cerebral disease, or coagulopathies.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00696618
Locations
| United States, Maryland | |
| Johns Hopkins University | |
| Baltimore, Maryland, United States, 21287 | |
Sponsors and Collaborators
Johns Hopkins University
University of California, Los Angeles
Investigators
| Principal Investigator: | Craig Hendrix, MD | Johns Hopkins University |
More Information
No publications provided
| Responsible Party: | Craig Hendrix, MD, Johns Hopkins University |
| ClinicalTrials.gov Identifier: | NCT00696618 History of Changes |
| Other Study ID Numbers: | NA_00010972 |
| Study First Received: | June 4, 2008 |
| Last Updated: | August 3, 2009 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Johns Hopkins University:
|
HIV prevention MSM Enema HIV Seronegativity |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases |
Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases Sodium phosphate Cathartics Gastrointestinal Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on June 18, 2013