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Scientists dig deep into HIV: tissue biopsies reveal hidden clues

NCT ID NCT00001471

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Sep 09, 2026 · Updated 13 times

Summary

This study collected tissue samples from the tonsils, lymph nodes, bowel, and lungs of HIV patients and healthy volunteers. The goal was to measure the amount of virus and certain immune cells in these tissues during treatment. By comparing samples, researchers hoped to learn more about how HIV affects the body beyond the blood.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

386 people

The number who actually took part.

Started

Nov 1994

Lead sponsor

A government research agency

The lead sponsor is the US National Institutes of Health.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

This study will include patients already seen in our outpatient clinic, as well as individuals recruited from outside clinics.

Ages

18 to 100 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

* INCLUSION CRITERIA: Greater than or equal to 18 years old. Ability to sign informed consent. For women of child-bearing potential, negative result on a serum or urine pregnancy test within 1 week prior to the procedure. Willingness to allow storage of blood or biopsy samples for possible future use to study HIV/AIDS, related diseases or the immune system; willingness to permit HLA testing. FOR PATIENTS UNDERGOING BIOPSIES: No medical contraindication to tonsillar, lymph node, or intestinal biopsy. For tonsillar biopsy, presence of visible tonsillar tissue; for lymph node biopsy, palpable lymph nodes. No aspirin or piroxicam (Feldene) for 10 days prior to the procedure; other non steroidal anti-inflammatory drugs (e.g. ibuprofen) must be discontinued the day prior to the procedure. Acetaminophen \[Tylenol\] is permitted at any time. FOR PATIENTS UNDERGOING BAL: Hematocrit greater than 27 percent, platelets greater than 50,000/ml. Baseline pulse-oximetry recording of 94 percent or greater unless clinical indication for bronchoscopy. No medical contraindication to bronchoscopy. In addition to the above: FOR HIV POSITIVE VOLUNTEERS: HIV infection must be confirmed by ELISA and western blot or dot blot. For patients with acute HIV infection and negative HIV serology, plasma HIV viral load greater than 10,000 copies/ml. FOR HEALTHY VOLUNTEERS: No underlying significant medical problem, especially an immunodeficiency or autoimmune disease, or an underlying problem requiring immunosuppressive therapy. Absence of HIV infection as confirmed by negative ELISA and, if indicated, western blot or dot blot. FOR ICL PATIENTS: Patients must meet the definition of ICL according to the CDC criteria: documented absolute CD4 T lymphocyte count of less than 300 cells per cubic millimeter or of less than 20 percent of total T cells on more than one occasion usually two to three months apart, without evidence of HIV infection or any defined immunodeficiency or therapy associated with depressed levels of CD4 T cells. Absence of HIV infection as confirmed by negative ELISA and, if indicated, western blot or dot blot. EXCLUSION CRITERIA: FOR ALL VOLUNTEERS UNDERGOING BIOPSIES: Platelet count less than 75,000 platelets/mm(3). PT or PTT prolonged by greater than 2 seconds unless patient has documented lupus anticoagulant/anti-phospholipid syndrome, which is not associated with an increased bleeding risk Known underlying bleeding disorder. Pregnancy. FOR HIV-POSITIVE OR ICL VOLUNTEERS FOR LYMPH NODE BIOPSIES: Use of narcotics (other than as prescribed by a physician) or cocaine less than 1 week prior to the date of biopsy. FOR ALL VOLUNTEERS FOR INTESTINAL BIOPSIES: Use of narcotics (other than as prescribed by a physician) or cocaine less than 1 week prior to the date of biopsy. Significant heart valve abnormalities. Presence of pacemaker, artificial joint or vascular surgery graft. FOR ALL VOLUNTEERS FOR BAL: Use of narcotics (other than as prescribed by a physician) or cocaine less than 1 week prior to the date of biopsy. Pregnancy. Any medical condition for which the investigators believe bronchoscopy may be contraindicated. Allergy to lidocaine. History of asthma requiring therapy.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • National Institutes of Health Clinical Center

    Bethesda, Maryland, 20892, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.