Clinical trials

2

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

Condition / disease
Location
Status: Not yet recruiting

Effectiveness of Stress Management Training in Reducing Caregiver Burden and Perceived Stress in ICU Families

This research helps to close an important gap in the provision of care to ICU families and introduces a structured and accessible psychological intervention to family caregivers of long-stay ICU patients. The findings are expected to contribute to the integration of stress management training in family-centered nursing practices and contribute to improved psychological well-being of the caregivers of families in intensive care settings.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Al-Balqa Applied UniversityUpdated: Sep 10, 2026
Eligibility criteria

Aged 18 years or older. [+5]

A history of a psychiatric disorder that substantially impairs their ability to...

Status: Not yet recruiting

Intermittent Boluses Versus Infusion of Propofol During Gastroscopy

It is unclear whether continuous infusion or intermittent bolus injection of propofol is better for achieving adequate sedation during a standard upper endoscopy. The study aimed to compare the efficacy and safety of continuous infusion and intermittent bolus injection of Propofol (Diprivan) during a standard upper endoscopy. In this prospective study, patients will be randomly assigned to undergo a standard upper endoscopy with either continuous infusion (CI group) or intermittent bolus injection (BI group) of Propofol (Diprivan) administered by an anesthesiologist. The primary outcome will be to assess the quality of sedation by the endoscopist (VAS). In addition to other sedation-related parameters that will include sedation induction time (minutes), total dose of propofol (mg), recovery time (minutes) using Aldrete score, any involuntary patient movement, and adverse events.

Participants needed: 100
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: Al-Balqa Applied UniversityUpdated: Aug 7, 2024
Eligibility criteria

Patients of both genders [+2]

Patients who are pregnant, [+5]