Recruiting

Lyme Disease

Sponsor:

National Institute of Allergy and Infectious Diseases (NIAID)

Code:

NCT00028080

Conditions

Lyme Disease

Eligibility Criteria

Sex: All

Age: 2 - 70+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

This study is designed to establish a population of patients with Lyme disease for evaluation, treatment and follow-up to learn more about the infection.

Patients with active Lyme disease may be eligible for this study.

Participants will have a medical history and physical examination and diagnostic evaluations as appropriate to their individual condition. Laboratory tests may include routing blood and urine tests, X-rays, or other imaging studies, body fluid or tissue cultures, skin biopsy and tests for allergic or immune responses. Treatment will include only medications approved by the Food and Drug Administration, given according to accepted dose schedules and ways of taking the medicines. All diagnostic tests and treatments will be according to standard medical practice for the disease. No experimental procedures will be offered under this protocol.

Patients will be followed as needed for evaluation and treatment of their condition. In general, they will be asked to return at the end of therapy, then 3, 6 and 12 months later, and then every 6 to 12 months. More frequent visits may be required or less frequent visits may be allowed, depending on the individual s condition.

Participants may be asked to undergo the following additional procedures for research purposes:

  • Extra blood draws to study Lyme disease and other inflammatory conditions. Blood will be drawn from arm veins. The total amount drawn during any 6-week period will not exceed 450 cc (30 tablespoons) for adults and 7 cc (1/2 tablespoon) per kilogram (2.2 pounds) of body weight for children under 18 years of age.
  • Leukapheresis to collect large numbers of white blood cells. Whole blood is collected through a needle in an arm vein, similar to donating blood. The blood circulates through a machine that separates it into its components, and the white cells are removed. The rest of the blood is returned to the body through the same needle. Only adults 18 years of age and older will be asked to undergo leukapheresis.

Conditions

Lyme Disease

Study ID

NCT00028080

Start date

Jan 16, 2002

Status verified date

Jul 28, 2026

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 2 - 70+

Healthy Volunteers: Not accepted

  • INCLUSION CRITERIA:
  • Clinical diagnosis of active Lyme disease at the time of the initial NIH evaluation based on the CDC case definition. Study physician will review history to confirm probable cases.
  • Subjects must maintain a private physician for non-protocol related medical complaints and for emergency medical treatment required for these or other of their disorders.

EXCLUSION CRITERIA:

  • Post treatment Lyme disease syndrome.
  • Unacceptably poor compliance, which, in the opinion of the investigator, would interfere with one's ability to study or provide quality medical care for the patient.

ELIGIBILITY CRITERIA TO BE ASKED TO UNDERGO APHERESIS INCLUDE:

  • Age 18 years or above
  • Weight greater than 110 pounds
  • No known heart, lung, kidney disease, or bleeding disorders
  • Negative HIV, HCV and HBsAg serologies
  • Female subjects should not be pregnant or nursing
  • Adequate peripheral venous access

Patients will have a CBC performed up to 2 weeks before the procedure. In order to be able to undergo the procedure, patient must fulfill all of the below:

  • Hemoglobin greater than 11 g/dL for males and greater than 10 g/dL for females
  • Platelets greater than 150 k/mm(3)
  • WBC greater than 3.5 x 10(3) uL
  • MCV above 80

Women who are able to conceive children must have a negative pregnancy test within 2 weeks before the procedure.

Study Design

Enrollment

500 participants

Anticipated

Interventions and Outcome Measures

Arms

Lyme Disease

Participants who have been diagnosed with or are strongly suspected to have Lyme disease.

Primary outcome measure

  • Develop a defined population of patients with Lyme disease to serve as the basis of research in multiple aspects of the infection. [ Time Frame: 12/31/2030 ]

Central Contacts and Locations

Central contacts

Locations

National Institutes of Health Clinical Center

Recruiting

Bethesda, Maryland, United States, 20892

Contacts

For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR)

800-411-1222ccopr@nih.gov

More Information

Sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Last update posted

Aug 7, 2026

Last verified

Jul 28, 2026

Keywords

  • Borrelia Burgdorferi
  • Lyme Disease
  • Infection
  • Therapy
  • Natural History
  • Lyme

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by National Institute of Allergy and Infectious Diseases (NIAID) on 2026-08-07.