Clinical trials

6

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

Effect of Tourniquet Use on the Pivot Shift Test

This prospective study will evaluate whether tourniquet inflation affects the results of the pivot shift test in patients undergoing anterior cruciate ligament (ACL) reconstruction. The pivot shift test is commonly used to assess rotational instability of the knee in patients with ACL injury. In each participant, the pivot shift test will be performed under anesthesia before and after inflation of the thigh tourniquet, allowing the two conditions to be compared within the same patient. The study aims to determine whether tourniquet use changes the findings of the pivot shift examination. Understanding the possible influence of tourniquet inflation may help standardize intraoperative assessment of rotational knee instability and improve interpretation of the pivot shift test during ACL surgery.

Participants needed: 34
Trial details
Age: 16-65Biological sex: AllType: InterventionalSponsor: Umraniye Education and Research HospitalUpdated: Sep 22, 2026Locations: 1
Eligibility criteria

Patients with anterior cruciate ligament (ACL) rupture. [+1]

Patients with multiligament knee injuries. [+1]

Status: Recruiting

Paragastric Block for Pain and PONV in Sleeve Gastrectomy

This single-center, prospective, randomized, double-blind controlled trial aims to evaluate the effects of intraoperative paragastric block (PGBLOCK) on early postoperative visceral pain, postoperative nausea and vomiting (PONV), and analgesic requirements in patients undergoing laparoscopic sleeve gastrectomy (LSG). Despite advancements in multimodal analgesia protocols, visceral pain remains a significant postoperative concern following LSG, contributing to increased opioid use and delayed recovery. Paragastric block is a novel technique targeting autonomic neural pathways-such as branches of the celiac ganglia and vagal nerves-through precise intraoperative injection of local anesthetics near the stomach. A total of 180 patients scheduled for elective LSG will be randomized in a 1:1 ratio to receive either paragastric block with 20 mL of 0.5% bupivacaine or a sham block with 20 mL of isotonic saline. Injections will be administered at six predefined anatomical sites under laparoscopic guidance after gastric resection. The surgical technique, anesthetic protocol, and postoperative care will be standardized for all participants. Both patients and clinical personnel involved in care and outcome assessment will remain blinded to group assignment. The primary outcome is the assessment of postoperative visceral pain using Visual Analog Scale (VAS) scores at 0 and 2 hours postoperatively. Secondary outcomes include PONV severity grading, mobilization status, total analgesic consumption (pethidine + tramadol), and need for rescue antiemetics within the first 24 hours post-surgery. Exclusion criteria include history of upper abdominal surgery, chronic opioid use, pregnancy, severe systemic disease, or allergy to medications used in the protocol. This study is expected to provide high-quality evidence regarding the efficacy of paragastric block in improving early postoperative recovery and reducing opioid reliance after LSG.

Participants needed: 200
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Umraniye Education and Research HospitalUpdated: Dec 18, 2025Locations: 1
Eligibility criteria

Patients aged between 18 and 65 years. [+3]

History of prior upper abdominal surgery. [+7]

Status: Recruiting

The Effects of VC Versus PC Ventilation on Cerebral and Respiratory Parameters in Patients Undergoing Laparoscopic Gynecologic Surgery

The aim of the study was to determine whether the use of different mechanical ventilation modes in patients with Trendelenburg position and CO2 insufflation affects respiration and cerebral oxygenation due to postoperative atelectasis, and was to determine whether there was any hemodynamic effect.

Participants needed: 120
Trial details
Age: 18-70Biological sex: FemaleType: InterventionalSponsor: Umraniye Education and Research HospitalUpdated: Nov 19, 2025Locations: 1
Eligibility criteria

18-70 age [+1]

Under 18 years of age, over 70 years of age, [+7]

Status: Recruiting

Effects of Malnutrition on Respiratory and Renal Functions in Patients Undergoing Peroral Endoscopic Myotomy (POEM)

The hypothesis of this study is to investigate cardiorespiratory and renal complications in patients under general anesthesia undergoing POEM surgery.

Participants needed: 60
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Umraniye Education and Research HospitalUpdated: Nov 19, 2025Locations: 1
Eligibility criteria

Patients diagnosed with achalasia and suitable for POEM treatment by gastroenter... [+2]

Those with a known history of active lung infection, advanced COPD, or respirato... [+9]

Status: Not yet recruiting

Low and Moderete Flow Anaesthesia on Haemodynamics

The study topic investigates the potential advantages of low-flow anesthesia in terms of physiological protection and resource saving.

Participants needed: 76
Trial details
Age: 17-70Biological sex: AllType: InterventionalSponsor: Umraniye Education and Research HospitalUpdated: Mar 11, 2025Locations: 1
Eligibility criteria

being ASA1-2 status [+2]

Patients who refuse to give informed consent [+5]

Status: Not yet recruiting

Effectiveness of Bilateral Endoscopic Sphenopalatine Ganglion Block on Postoperative Pain After Septoplasty

The aim of this clinical study will investigate the efficacy of sphenopalatine ganglion block in the treatment of postoperative pain.it will also be learnt whether it reduces the consumption of analgesics in postoperative pain.The main questions it aims to answer are: Will the participants' need for painkillers decrease after the operation? Can sphenopalatine ganglion block be used for postoperative pain after septoplasty? The researchers will compare 2 groups with and without sphenopalatine ganglion block to see the effectiveness of sphenopalatine ganglion block. Participants will: Read the information Participants have been given about the sphenopalatine ganglion block. In case of any side effects, please contact participant's doctor.

Participants needed: 50
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: Umraniye Education and Research HospitalUpdated: Nov 19, 2024
Eligibility criteria

Participants who will undergo septoplasty [+2]

Under 18 or over 50 years of age [+8]