Clinical trials

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Condition / disease
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Status: Not yet recruiting

ComBaCaL HIV Prevention TwiCs

This cluster-randomized intervention is embedded in the ComBaCaL (Community-Based Chronic disease care Lesotho) cohort study (EKNZ ID AO\_2022-00058, clinicaltrials.gov ID NCT05596773, Lesotho NH-REC ID 210-2022), a platform for the investigation of chronic diseases and their management in rural Lesotho that is maintained by local lay chronic care village health workers (CC-VHWs). This study is to evaluate the effectiveness and safety of the CoPrev model in regard to biomedical HIV prevention utilization compared with an enhanced standard of care, in which VHWs assisted by a tablet-based CDS application, perform the same activities except for the prescription and/or delivery of PEP, oral PrEP, COC and self-injectable contraception. Additionally, this study aims to assess the outcomes and processes related to the implementation of such a model.

Participants needed: 380
Trial details
Age: 15+Biological sex: AllType: InterventionalSponsor: University Hospital, Basel, SwitzerlandUpdated: May 22, 2026Locations: 2
Eligibility criteria

Participant of the ComBaCaL cohort study (signed informed consent available) [+10]

Known allergies to PEP/oral PrEP [+1]

Status: Recruiting

Community-Based Chronic Disease Care in Rural Lesotho

This ComBaCaL cohort study is to assess the impact of community-based, lay-led chronic disease screening and care interventions in rural Lesotho. It aims to establish a prospective research and service delivery platform in rural Lesotho that is managed by eHealth-supported Chronic Care Village Health Worker (CC-VHWs) providing regular chronic disease screening, monitoring and referral services. The implementation outcomes of the cohort as well as the effect of the cohort activities on disease-specific care cascades will be assessed. Subsequently, nested trials to assess the effectiveness of specific chronic disease control interventions will be developed. Measurements and data entry will be conducted by CC-VHWs. The CC-VHWs will be equipped with the essential tools required for chronic disease monitoring in the community (i.e. BP machines, scales, measuring band, glucometers, and urine dipsticks). They will undergo a theoretical and practical training covering all aspects required for correct data collection and chronic disease screening, diagnosing, referral and counselling services. At every visit, the CC-VHW will screen participants for warning signs and symptoms (i.e. shortness of breath, severe headache, chest pain, new-onset confusion, impaired consciousness, severely impaired general state of health) and refer participants to the closest health centre in case of any danger-sign. The CC-VHWs will be continuously monitored and supervised by health centre nurses of the respective village's catchment area, mainly through direct interaction during monthly VHW meetings and by CC nurses through field visits, remote interaction via phone calls or messages sent via the ComBaCaL app and through direct contact during the monthly VHW meetings at the health centre. The CC-VHWs are embedded within the Lesotho MoH VHW program and may during the project period be trained and equipped to provide further routine services in their communities.

Participants needed: 17,500
Trial details
Biological sex: AllType: ObservationalSponsor: University Hospital, Basel, SwitzerlandUpdated: Feb 13, 2026Locations: 2
Eligibility criteria

Village size of 40 to 100 households [+14]

Status: Recruiting

Investigating the Optimal Management of Dolutegravir Resistance

The goal of this study is to address the gap in published data on viral suppression among people meeting the criteria for virologic failure on dolutegravir (DTG)-based ART regimens without a change in regimen. The study will also assess the emergence of DTG-associated drug-resistant mutations and their impact on viral suppression.

Participants needed: 6,600
Trial details
Age: 1+Biological sex: AllType: ObservationalSponsor: University of NairobiUpdated: Sep 5, 2025Locations: 9
Eligibility criteria

Able and willing to provide informed consent (assent as appropriate and legal gu... [+4]

Has switched ART regimen for confirmed or suspected HIV treatment failure while... [+2]

Status: Recruiting

Ndovu RCT: Investing the Optimal Management of Dolutegravir Resistance

This clinical trial will address the gap in published data on the effect of dolutegravir (DTG)-associated drug-resistant mutations on viral suppression among people remaining on DTG-based antiretroviral therapy. It will also address the gap in the optimal management strategy for this population.

Participants needed: 392
Trial details
Phase: Phase 3Age: 3+Biological sex: AllType: InterventionalSponsor: University of NairobiUpdated: Sep 11, 2025Locations: 9
Eligibility criteria

Enrolled in the Ndovu cohort study [+5]

Pregnant or breastfeeding [+4]