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NCT ID: NCT00522912 Completed - Clinical trials for Trachomatous Trichiasis

A Trial of Epilation Verses Surgery for Minor Trichiasis

Start date: March 2008
Phase: N/A
Study type: Interventional

Trachoma is the leading infectious cause of blindness worldwide. Recurrent infection by Chlamydia trachomatis causes a gradual scarring process of the inner surface of the eyelid (conjunctiva) leading to in-turning of the eyelids (entropion) and lashes touching the eye (trichiasis). The rate of progression and the severity of disease are variable. Some people develop severe disease with extensive entropion and trichiasis, whilst others have a mild problem with only a few lashes touching the eye, which does not progress. In more advanced cases there is a broad consensus that the entropion / trichiasis should be corrected by surgery. In mild cases (minor trichiasis: 1-5 lashes touching the eye) the optimal treatment is uncertain. Some advocate early surgery to turn the eyelid out for any individual with one or more lashes touching any part of the eye. Others consider this to be too early for surgical intervention, as surgery can have a high recurrence rate and complications can arise. Instead, they recommend that minor trichiasis can be managed by epilation (pulling out lashes with forceps). In many endemic regions the uptake of surgery is low, with many patients preferring to epilate for mild disease. The primary purpose of this study is to compare the outcome of immediate surgery to regular epilation for the management of minor trichiasis. The epilation would be done by a person with good eyesight using proper epilation forceps.

NCT ID: NCT00522860 Completed - Trachoma Clinical Trials

A Trial of Non-absorbable Versus Absorbable Sutures for Trichiasis Surgery

Start date: March 2008
Phase: Phase 4
Study type: Interventional

Trachoma is the leading infectious cause of blindness worldwide. Recurrent infection by Chlamydia trachomatis causes in-turning of the eyelids / lashes (trichiasis), leading to corneal damage and blindness. The WHO recommends corrective eyelid surgery for trichiasis. Unfortunately, trichiasis frequently returns following surgery. The purpose of this study is to compare the outcome of surgery (at one and two years) for trichiasis using two currently used alternative suture types: non-absorbable (silk) and absorbable (vicryl). We, the researchers, hypothesise that the supportive presence of the absorbable suture for a longer period produces more stable wound healing, leading to a better outcome.

NCT ID: NCT00456469 Not yet recruiting - Tuberculosis Clinical Trials

Diagnosis of Active and Latent TB Infection With IFN-y Assays in African Children

ALTAC
Start date: May 2007
Phase: N/A
Study type: Observational

Study based in Southern Ethiopia Purpose - to explore if children in contact with adults with TB have positive acute reactants such as IFN-y and other cytokine responses; if these responses discriminate between high and low risk of disease progression and whether these could be incorporated into improved diagnostic approaches.

NCT ID: NCT00451139 Completed - Malaria Clinical Trials

Ototoxicity of Artemether / Lumefantrine (Coartem) and Other Antimalarials

Start date: n/a
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate the potential side-effects of artemether / lumefantrine and other antimalarials on the auditory function.

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: NCT00255567 Completed - Clinical trials for Visceral Leishmaniasis

Efficacy/Safety of Sodium Stibogluconate (SSG) Versus Paromomycin (PM) and SSG/PM Combination to Treat V Leishmaniasis

Start date: November 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of SSG 30 days alone, PM 21 days alone and SSG and PM as a combination course of 17 days in the treatment of patients with VL.

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.

NCT ID: NCT00074399 Completed - HIV Infections Clinical Trials

Nevirapine (NVP) Use to Prevent Mother-to-Child Transmission of HIV

Start date: February 2001
Phase: Phase 3
Study type: Interventional

HIV can be transmitted from an HIV infected mother to her infant through her breast milk. The purpose of this study is to determine whether giving infants of HIV infected mothers the anti-HIV drug nevirapine (NVP) for six weeks will reduce the risk of HIV transmission. Study hypothesis: Six weeks of nevirapine prophylaxis provided to the infant will decrease HIV transmission through breastfeeding.

NCT ID: NCT00002399 Completed - HIV Infections Clinical Trials

A Comparison of SCH 56592 and Fluconazole in the Treatment of Oropharyngeal Candidiasis (OPC) in HIV-Positive Patients

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the safety and effectiveness of SCH 56592 with that of fluconazole in the treatment of OPC (a fungal infection of the throat) in HIV-positive patients.