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Chlamydia clinical trials

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NCT ID: NCT01439503 Completed - HIV Infections Clinical Trials

Safer Sex Program for Young African-American Men

Start date: September 2012
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy of the adapted program a randomized controlled trial enrolling 620 eligible African American men who have sex with men (MSM) will be conducted. Men in the treatment condition will be compared to men receiving the control condition comprised of standard of care counseling from the clinic plus a free bag of condoms and water-based lubricants. This two-arm trial will test four hypotheses: Aim: To test the efficacy of a brief, clinic-based and theory-guided, intervention designed to reduce STD incidence and risk of HIV acquisition/transmission among young African American men (15-29 years old) having sex with men and presenting for STD testing. H1. Men randomized to receive the intervention will have a lower incidence rate of laboratory-confirmed STDs at each of three follow-up assessments compared to those receiving the control condition. H2. Men randomized to receive the intervention will report significantly fewer acts of unprotected penetrative sex (penile-vaginal or penile-anal) between follow-up assessments compared to those receiving the control condition. H3. Men randomized to receive the intervention will report having significantly fewer unprotected penetrative sex partners (for penile-vaginal or penile-anal sex) between follow-up assessments compared to those receiving the control condition. H4. Men randomized to receive the intervention will report having significantly fewer negative experiences with condom use between follow-up assessments compared to those receiving the control condition. H5. Men randomized to receive the intervention will demonstrate significantly greater improvement in condom application skills, throughout the 12-month study, compared to those receiving the control condition.

NCT ID: NCT01202331 Completed - Chlamydia Clinical Trials

Tripartite International Research for the Elimination of Trachoma

TIRET
Start date: November 2010
Phase: Phase 4
Study type: Interventional

Mass antimicrobial administrations have been remarkably successful in reducing the prevalence of the ocular strains of Chlamydia that cause trachoma. Repeated distributions progressively lower the prevalence of infection, and in some cases may even result in local elimination. Mass treatments cannot be continued forever, due to concerns about cost and antibiotic resistance. The hope has been that other measures such as latrine construction and hygiene programs would prevent infection from returning. Unfortunately, no non-antibiotic measure has yet demonstrated an effect on infection. 1. We hypothesize that Chlamydial infection will return to communities when treatment ends. 2. We hypothesize that infection will be completely eliminated in all communities treated for seven years. 3. We hypothesize that identifying and treating clinically active cases among preschool aged children will delay or even prevent reemergence at a far lower cost than mass treatment of all individuals.

NCT ID: NCT01184157 Completed - Gonorrhea Clinical Trials

Randomized Trial of Home Versus Clinic-based Screening for Sexually Transmitted Infections

Start date: n/a
Phase: N/A
Study type: Interventional

This study randomizes women using long-acting reversible methods of contraception to home-based STD screening through the mail compared to screening available in a clinical setting. We hypothesize that women randomized to home-based screening will be more likely to complete screening.

NCT ID: NCT01150747 Completed - Chlamydia Clinical Trials

Chlamydia Trachomatis Immunology and Vaccinology Study

Start date: January 2011
Phase: N/A
Study type: Observational

The primary objective is to prospectively follow 200 women with or at risk of cervicitis to determine the chlamydia-specific cellular responses that correlate with protection against incident infection. The hypothesis is that a positive IFN-y response by peripheral CD4+ T cells responding to stimulation with HSP60 will be significantly associated with protection from incident C. trachomatis infection.

NCT ID: NCT01140022 Completed - Chlamydia Clinical Trials

Leveraging Technology as a Clinician Extender to Screen Culturally Diverse Young Women for Chlamydia

Start date: September 2007
Phase: N/A
Study type: Observational

The purpose of this study is to conduct a quality improvement intervention to improve the ability of health care providers to deliver an important preventive health service (CT screening) in order to meet the goal of universal CT screening for young women age 25 or younger as recommended by the CDC and virtually all major health organizations. This novel approach utilizes a bilingual (English-Spanish) computer kiosk module to deliver education about CT and allow patients to request a CT screening test. This module should significantly increase CT screening among at risk women (18-25yo) attending urgent care clinics and emergency departments.

NCT ID: NCT00970749 Completed - Chlamydia Clinical Trials

Antigen-Specific Cell Mediated Immune Response to Chlamydia Trachomatis

Start date: December 2009
Phase: N/A
Study type: Observational

This is an exploratory study in which the investigators will develop a way to identify the cell responses most strongly associated with protection against chlamydia infection. This study is not driven by a hypothesis.

NCT ID: NCT00827697 Completed - Gonorrhea Clinical Trials

A Validation Study for Detecting Chlamydia and Gonorrhea in Rectal Samples

Start date: May 2009
Phase: N/A
Study type: Observational

Our hypothesis is that nucleic acid amplification testing (NAAT) with the APTIMA Combo2 (AC2) will have greater sensitivity than culture in detecting Neisseria gonorrhoeae in rectal samples. We also hypothesize that AC2 will be equivalent to NAAT with the Becton Dickinson ProbeTec in detecting Chlamydia trachomatis and Neisseria gonorrhoeae in rectal samples.

NCT ID: NCT00644150 Completed - HIV Infections Clinical Trials

Effectiveness of HIV/Sexually Transmitted Infection Training for Physicians in China

Start date: April 2007
Phase: N/A
Study type: Interventional

This study will evaluate the effectiveness of a physician training program, the Ai Shi Zi program, in improving HIV/sexually transmitted infection diagnosis, treatment, and management by Chinese physicians and in reducing the number of subsequent infections in their patients.

NCT ID: NCT00322972 Completed - Chlamydia Clinical Trials

Trachoma Amelioration in Northern Amhara (TANA)

TANA
Start date: June 2006
Phase: Phase 4
Study type: Interventional

The WHO has initiated a program to eliminate trachoma, blinding eye infection caused by Chlamydia trachomatis, in large part by mass distributions of oral azithromycin. The proposed study will determine the frequency and treatment target of community-wide mass antibiotic treatment. We will also study the impact of mass antibiotic distribution on antibiotic-resistance in pneumococcus.

NCT ID: NCT00221364 Completed - Chlamydia Clinical Trials

Trachoma Elimination Follow-up

TEF
Start date: March 2003
Phase: Phase 4
Study type: Interventional

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.