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HIV-discordant Couple Intrauterine Insemination

Primary Purpose

Infertility, HIV Infections

Status
No longer available
Phase
Locations
United States
Study Type
Expanded Access
Intervention
Sperm washing and testing for HIV contamination
Intrauterine Insemination
Sponsored by
University of Missouri-Columbia
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an expanded access trial for Infertility focused on measuring fertility, HIV discordant, HIV, Infertility in HIV-discordant couples, HIV seronegativity

Eligibility Criteria

18 Years - 38 Years (Adult)All Sexes

Inclusion Criteria:

Couple must:

  • attest to safe sex practices
  • know the HIV-status of their partner
  • be informed of risks of this procedure and alternatives, including donor insemination
  • have the ability to provide informed consent
  • been referred or self-refer to Dr. Schust for infertility treatment

Female must:

  • be 18-38 years of age
  • have a normal menstrual cycle before the IUI cycle
  • be negative for HIV, gonorrhea, chlamydia, syphilis, hepatitis B and hepatitis C
  • have a standard infertility evaluation and be a candidate for intrauterine insemination

Male must:

  • be at least 18 years of age
  • be HIV-seropositive
  • be under the care of an infectious disease specialist
  • disease must be under control without evidence of acquired immunodeficiency syndrome (AIDS), with viral load <50,000 copies/mL and CD4 count > 250 cells/mL for the preceding 6 month period
  • have semen quality adequate for intrauterine insemination

If the couple does not achieve pregnancy after IUI, they may continue in the study for 5 additional treatment subsequent cycles. The man must continue to receive care for his HIV and the disease must continue to be under control. Before each cycle of insemination, the couple must each sign an attestation statement that he/she is following safe sex practices, and have repeat testing for sexually-transmitted infections.

Sites / Locations

  • Missouri Center for Reproductive Medicine & Fertility

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
September 10, 2009
Last Updated
November 30, 2015
Sponsor
University of Missouri-Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT00975546
Brief Title
HIV-discordant Couple Intrauterine Insemination
Official Title
Intrauterine Insemination for HIV-discordant Couples
Study Type
Expanded Access

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
No longer available
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Missouri-Columbia

4. Oversight

5. Study Description

Brief Summary
The investigators propose to treat couples who wish to have a child in which the man is HIV-positive and the woman is HIV-negative. The investigators call these couples HIV-discordant. On the average, an HIV-positive man, who does not participate in high-risk activities, will transmit HIV to a female partner one in every one thousand acts of intercourse without a condom. To reduce transmission of HIV, HIV-discordant couples are counseled to avoid intercourse altogether, or to use condoms during every act of intercourse. In order to have a child, these patients can use donor insemination. If they wish to have a natural child of the infected man, they can use a combination of medication of the man to reduce the amount of virus in his semen, and condom use except at the time of ovulation when the woman produces an egg. This reduces the chance of infecting the woman, but studies have shown that about 4% of women will be infected with HIV using this approach. Alternatively, they can use vitro fertilization (IVF) with intra cytoplasmic sperm injection (ICSI) in which eggs are collected from the woman after hormone-stimulation and are fertilized in the laboratory by injecting a single washed sperm from her husband into each egg. The resulting embryos can be transferred to the wife's uterus and/or frozen for later use. These procedures are believed to minimize the risk of HIV transmission (although the number of cases is low), but IVF-ICSI is very expensive and are not an option for everyone. A simpler method used for over 15 years in Europe is to collect the man's semen, wash the sperm in the laboratory, and test the sperm sample for HIV before placing it in the woman's uterus (intrauterine insemination; IUI). Although the risk of HIV transmission to the woman is presumably not zero with this method, over 4000 inseminations reported have not resulted in infection of any female patients or resulting children.
Detailed Description
This study will enroll couples who wish to have a child in which the man is HIV-seropositive and the woman is HIV-seronegative. The couple will be counseled about their reproductive options, including in vitro fertilization (IVF) donor insemination and adoption. The male patient will be using appropriate therapy to reduce the virus in his semen. Semen will undergo specialized washing to reduce viral contamination of sperm. The sperm are first separated from leukocytes and other seminal constituents by centrifugation over a stepwise gradient. Motile sperm will be separated from the resulting pellet by a swim-up step in which washed sperm are overlaid with fresh medium into which sperm migrate. The final sperm suspension will be stored while testing for HIV is performed by reverse transcription polymerase chain reaction (RT-PCR). Specimens found negative for HIV will then be used for IUI (review: Gilling-Smith et al, 2006; Bujan et al 2007). There is presumably some risk of HIV transmission to the woman and resulting child with this approach; however, over 4000 inseminations reported in Europe over the last 15 years have not resulted in infection of any female patient or resulting child. The woman will be followed for a year after the final IUI to assess seroconversion. If a child is born, he or she will be tested for HIV at 3 months of age.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, HIV Infections
Keywords
fertility, HIV discordant, HIV, Infertility in HIV-discordant couples, HIV seronegativity

7. Study Design

8. Arms, Groups, and Interventions

Intervention Type
Other
Intervention Name(s)
Sperm washing and testing for HIV contamination
Intervention Description
Semen will undergo specialized washing to reduce viral contamination of sperm. The sperm are first separated from leukocytes and other seminal constituents by centrifugation over a stepwise gradient. Motile sperm will be separated from the resulting pellet by a swim-up step in which washed sperm are overlaid with fresh medium into which sperm migrate. The final sperm suspension will be stored while testing for HIV is performed by reverse transcription polymerase chain reaction (RT-PCR)
Intervention Type
Procedure
Intervention Name(s)
Intrauterine Insemination
Intervention Description
Intrauterine Insemination (IUI) will be performed on the HIV-negative wife, following standard clinical practice, using washed sperm from her HIV-positive husband after testing the IUI sample for HIV.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
38 Years
Eligibility Criteria
Inclusion Criteria: Couple must: attest to safe sex practices know the HIV-status of their partner be informed of risks of this procedure and alternatives, including donor insemination have the ability to provide informed consent been referred or self-refer to Dr. Schust for infertility treatment Female must: be 18-38 years of age have a normal menstrual cycle before the IUI cycle be negative for HIV, gonorrhea, chlamydia, syphilis, hepatitis B and hepatitis C have a standard infertility evaluation and be a candidate for intrauterine insemination Male must: be at least 18 years of age be HIV-seropositive be under the care of an infectious disease specialist disease must be under control without evidence of acquired immunodeficiency syndrome (AIDS), with viral load <50,000 copies/mL and CD4 count > 250 cells/mL for the preceding 6 month period have semen quality adequate for intrauterine insemination If the couple does not achieve pregnancy after IUI, they may continue in the study for 5 additional treatment subsequent cycles. The man must continue to receive care for his HIV and the disease must continue to be under control. Before each cycle of insemination, the couple must each sign an attestation statement that he/she is following safe sex practices, and have repeat testing for sexually-transmitted infections.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Danny J Schust, MD
Organizational Affiliation
University of Missouri-Columbia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Erma Z Drobnis, PhD
Organizational Affiliation
University of Missouri-Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Missouri Center for Reproductive Medicine & Fertility
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65201
Country
United States

12. IPD Sharing Statement

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HIV-discordant Couple Intrauterine Insemination

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