Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Accelerated Treatment of Depressive Patients With tDCS

A randomized, controlled three-arm study is planned to investigate the effectiveness and feasibility of an accelerated home-based tDCS application (3 weeks of transcranial direct current stimulation at home, twice daily). A total of 30 patients with depression (10 per group), who are currently not taking and have no history of taking antidepressant medication, will be randomly assigned to either an active tDCS condition, a sham (placebo) tDCS condition, or a waitlist control group. The latter two groups will receive active tDCS treatment after completion of the control phase. This study represents a continuation of the pilot study GSUND DAHOAM (Ethics approval: 20-2091-101; Dragon et al., 2024).

Participants needed: 30
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: University of RegensburgUpdated: Jun 15, 2026Locations: 1
Eligibility criteria

Sex: female, male, non-binary [+4]

Presence of contraindications for tDCS (e.g., electrical implants or metallic ob... [+3]

Status: Recruiting

A Trial to Assess Haploidentical T-depleted Stem Cell Transplantation in Patients With SCD

HSCT is currently the only curative option for SCD but less than 20% of SCD patients have a MD donor available. So far, all curative approaches beyond a MSD HSCT at young age are non-satisfactory. With the lack of a suitable donor for the vast majority of patients, the major question of this trial is, if a haploidentical αß/CD19+ T-cell depleted HSCT can be a valid alternative to a MSD HSCT. The main challenge in non-malignant diseases is to offer a safe and GvHD-free HSCT without rejection.

Participants needed: 212
Trial details
Phase: Phase 2Age: 2-35Biological sex: AllType: InterventionalSponsor: University of RegensburgUpdated: May 13, 2024Locations: 9
Eligibility criteria

Age 2yrs to 35yrs [+15]

Karnofsky or Lansky Performance Score < 70% [+24]

Status: Recruiting

Longitudinal Study of CRS/HIPEC for Peritoneal Carcinomatoses

Longitudinal Study of the Effect of Cytoreductive Surgery and HIPEC in Patients With Peritoneal Carcinomatoses

Participants needed: 250
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: University of RegensburgUpdated: Aug 23, 2022Locations: 2
Eligibility criteria

suspicious peritoneal carcinomatosis

<18 years