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Effect of Seminal Fluid on the Colon Wall; Implications for HIV Transmission

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Johns Hopkins University

Status

Completed

Conditions

Human Immunodeficiency Virus (HIV)

Treatments

Biological: Radiolabeled Normosol-R
Biological: Radiolabeled autologous seminal fluid

Study type

Interventional

Funder types

Other

Identifiers

NCT01053741
NA_00014051

Details and patient eligibility

About

This research is being done to learn how seminal fluid affects the lining of the colon, and whether this might make it easier for HIV to get into the body and cause infection.

Full description

Design of effective rectal microbicides to prevent HIV infection requires an understanding of rectal HIV transmission and the location within the lower gastrointestinal (GI) tract (luminal and mucosal) of HIV (cell-free and cell-associated) following exposure to infected seminal fluid. These basic details of HIV transmission have yet to be determined in human subjects, yet they are essential to select microbicide candidates if they are to be rationally designed to achieve effective concentrations at sites of HIV transmission. Rational development of a rectal microbicide also requires an understanding of those factors that may contribute to colonic mucosal injury - potential confounders of microbicidal effect. Such factors include exposure to seminal fluid which has been shown in animal and in vitro studies to cause histologic and permeability changes that might facilitate HIV transmission.

Enrollment

11 patients

Sex

Male

Ages

21+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Able to provide signed informed consent
  • Men of 21 years or older.
  • Prior history of receptive anal intercourse.
  • Laboratory values within the last 28 days:
  • Negative for HIV antibodies
  • Lymphocyte count within normal limits
  • Neutrophil count > 1,000 cells/ml
  • Cluster of Differentiation 4 (CD4) cell count > 500 cells/ml
  • Platelet count ≥ 150,000 cells/mm3
  • Prothrombin Time (PT) within normal limits
  • Partial thromboplastin time (PTT) within normal limits.
  • No childbearing intentions.

Exclusion criteria

  • Active anorectal disease or recent (3 months) anorectal surgery;
  • Diarrhea, defined as three or more loose stools per day, for at least three days prior to admission.
  • History of sleep apnea, or airway problems with previous sedation procedures.
  • History of significant adverse reaction to sedation medications.
  • Other history, including significant occupational radiation exposure, history of inflammatory bowel disease or any other diseases and lab results, such that, in the judgment of the investigator, study procedures are not considered safe for the subject's participation.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

11 participants in 2 patient groups

Seminal Fluid then Normosol
Experimental group
Description:
2.5 mL radiolabeled autologous seminal fluid administered rectally x1. Two week pause between interventions. Then 2.5 mL radiolabeled Normosol-R administered rectally X1.
Treatment:
Biological: Radiolabeled Normosol-R
Biological: Radiolabeled autologous seminal fluid
Normosol then Seminal Fluid
Experimental group
Description:
2.5 mL radiolabeled Normosol-R administered rectally x1. Two week pause between interventions. Then 2.5 mL radiolabeled autologous seminal fluid administered rectally X1.
Treatment:
Biological: Radiolabeled Normosol-R
Biological: Radiolabeled autologous seminal fluid

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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