Perioperative Anesthetic

2

Review clinical trials related to Perioperative Anesthetic. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Effect of a Preoperative Educational Video on Anxiety Levels

Preoperative anxiety is common among patients undergoing elective surgery and may negatively affect perioperative outcomes. This randomized controlled trial aims to evaluate the effectiveness of a short educational video in reducing preoperative anxiety. Participants will be assigned to one of three groups: a QR code-based video group, a tablet-based video group, or a control group receiving standard preoperative information. Anxiety levels will be assessed using the Amsterdam Preoperative Anxiety and Information Scale (APAIS). The secondary objective is to evaluate the utilization of QR code-based video education.

Participants needed: 360
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Aksaray University Training and Research HospitalUpdated: Jul 1, 2026
Eligibility criteria

Age 18 years or older. [+3]

Emergency surgery. [+3]

Status: Recruiting

Effects of Rectal Indomethacin Suppository on Postoperative CRBD in Patients Undergoing LRP

The postoperative incidence of catheter-related bladder discomfort (CRBD) ranges from 47% to 95%. It increases postoperative pain and agitation, thus requiring early intervention. Although a variety of drugs are used for the prevention or treatment of CRBD, the adverse reactions of most of these drugs have limited their clinical application. In long-term clinical practice, we found that indomethacin suppository has a good therapeutic effect on the discomfort of pelvic-related organs caused by nociceptive stimulation. However, its preventive effect on CRBD has not been reported yet. We hypothesized that indomethacin suppository has a preventive effect on postoperative CRBD. To verify this hypothesis, patients undergoing laparoscopic radical prostatectomy were enrolled in the study. Patients in the intervention group received 50 mg of indomethacin suppository via the rectal route immediately after surgery, while those in the control group received no treatment. The severity of CRBD, pain scores, consumption of analgesics, other perioperative adverse reactions, and patient satisfaction were observed and recorded at 0, 1, 2, and 6 hours after surgery.

Participants needed: 130
Trial details
Age: 18-80Biological sex: MaleType: InterventionalSponsor: Zhejiang UniversityUpdated: May 27, 2026Locations: 1
Eligibility criteria

Aged 18 to 80 years old (inclusive); [+3]

Pre-existing bladder diseases, such as overactive bladder (frequency of micturit... [+12]