TEF: Trachoma Elimination Follow-up

Sponsor
University of California, San Francisco (Other)
Overall Status
Completed
CT.gov ID
NCT00221364
Collaborator
(none)
20,000
1
25
798.9

Study Details

Study Description

Brief Summary

The WHO has initiated a program to eliminate blinding trachoma by the year 2020, in large part by mass oral azithromycin distributions. It is not clear how frequently or for how long these treatments are necessary. Here we assess the frequency and duration of treatment.

Condition or Disease Intervention/Treatment Phase
  • Drug: Mass treatment with oral azithromycin to an entire village
Phase 4

Detailed Description

40 villages in the Gurage Zone of Ethiopia were randomly assigned to biannual treatment, annual treatment, and a single treatment. Each treatment consisted of a single dose of oral azithromycin to the entire population over the age of 1 year (when the study was started, azithromycin had not yet been approved for ages below 1 year). We assess the prevalence the ocular chlamydia that causes trachoma in the peak prevalence age of 1-5 years at baseline, and 2, 6, 12, 18, and 24 months post treatment. An extension of the study monitors infection at 30 and 36 months post treatment. Untreated villages from the same area are enrolled in a step-wedge design to assess the presence of a secular trend. A random sample of those not within the 1-5 year old age group are examined to assess the prevalence of infection in the entire community.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20000 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Single
Primary Purpose:
Treatment
Official Title:
Trachoma Elimination With Repeated Mass Azithromycin Treatments
Study Start Date :
Mar 1, 2003
Actual Primary Completion Date :
Apr 1, 2005
Actual Study Completion Date :
Apr 1, 2005

Outcome Measures

Primary Outcome Measures

  1. The prevalence of ocular chlamydia infection in a village as determined by PCR []

Secondary Outcome Measures

  1. Clinical active trachoma, as determined by the WHO simplified grading system, by village []

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Year and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Age 1 to 5 years old in a village in the Gurage zone with endemic trachoma

Exclusion Criteria:

Refusal of village chief (for village inclusion), or refusal of parent or guardian (for individual inclusion)

Contacts and Locations

Locations

Site City State Country Postal Code
1 ORBIS-Ethiopia Addis Ababa Ethiopia

Sponsors and Collaborators

  • University of California, San Francisco

Investigators

  • Principal Investigator: Thomas M Lietman, MD, Proctor Foundation, UCSF

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT00221364
Other Study ID Numbers:
  • 10-02630
First Posted:
Sep 22, 2005
Last Update Posted:
Jul 15, 2015
Last Verified:
Jul 1, 2015
Keywords provided by University of California, San Francisco
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 15, 2015