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Laparoscopic Surgery clinical trials

View clinical trials related to Laparoscopic Surgery.

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NCT ID: NCT06396351 Completed - Clinical trials for Laparoscopic Surgery

Factors Affecting Abdominal Compliance During CO2 Insufflation in Laparoscopic Abdominal Surgery

Start date: August 1, 2022
Phase:
Study type: Observational

The authors aimed to evaluate factors influencing abdominal compliance in laparoscopic abdominal surgery.

NCT ID: NCT06394375 Completed - Clinical trials for Laparoscopic Surgery

Opioid Free Anesthesia in Abdominal Laparoscopic Surgery

Start date: July 1, 2023
Phase: Phase 2/Phase 3
Study type: Interventional

Effectiveness of opioid free anesthesia using Dexmedetomidine to inhibit nociception in abdominal laparoscopic surgery

NCT ID: NCT06385210 Completed - Clinical trials for Laparoscopic Surgery

Barriers to Routine Surgical Video Recording

Start date: April 1, 2024
Phase: N/A
Study type: Interventional

In order to improve the implementation of routine surgical video recording, the researchers want to understand what the challenges associated with the uptake of this technology are. The aim of this study is to explore the barriers faced by key stakeholders including the surgical care team, information governance, and patients within the field of surgical video reporting. The data from this qualitative study will allow the researchers to understand better the challenges associated with uptake of surgical video recording. This will allow the researchers to develop strategies to overcome these challenges and subsequently improve uptake of surgical video recording which will promote safer and more transparent surgery.

NCT ID: NCT05624346 Completed - Clinical trials for Laparoscopic Surgery

The Effect of Respiratory Exercise After Laparoscopic Surgery

Start date: September 26, 2022
Phase: N/A
Study type: Interventional

Laparoscopic surgery (LS) enables the patient to experience the desired result with smaller incisions in the postoperative period, more aesthetically, stress-free and less painful. This increases patient satisfaction and reduces morbidity and mortality. In the literature, it has been stated that respiratory exercises reduce the level of anxiety in different patient groups in the postoperative period and increase the quality of sleep and recovery. Among the duties and responsibilities of nurses working in surgical clinics are to provide breathing exercise training to patients in the preoperative period and to ensure that it is applied in the postoperative period. This study was planned to determine the effect of respiratory exercise applied to laparoscopic surgery patients on postoperative pain, anxiety, nausea-vomiting and respiratory parameters.

NCT ID: NCT05565508 Completed - Clinical trials for Laparoscopic Surgery

Safe Laparoscopic Access in Patients With Previous Abdominal and Pelvic Surgery

Start date: March 20, 2020
Phase: N/A
Study type: Interventional

the study discussed the safety of new technique for primary port insertion in cases of previous abdominal and pelvic surgery

NCT ID: NCT05540236 Completed - Clinical trials for Laparoscopic Surgery

Effects of Auricular Acupressure on the Management of Postoperative Nausea and Vomiting After Gynecological Laparoscopic Surgeries

Start date: July 18, 2021
Phase: N/A
Study type: Interventional

Auricular acupressure is easily accessible and easily performed, and can significantly relieve PONV symptoms, and improve patient's satisfaction in women receiving general anesthesia for gynecological surgeries. This makes it an economically-beneficial supplemental therapy, worthy of promoting for patients receiving general anesthesia.

NCT ID: NCT05475470 Completed - Safety Issues Clinical Trials

Blade Finger Technique for Safe Laparoscopic Entery

new technique
Start date: March 20, 2020
Phase: N/A
Study type: Interventional

blade-finger technique is a new technique for laparoscopic access which is safe

NCT ID: NCT05283733 Completed - Sepsis Clinical Trials

Open to Laparoscopic Reverse Conversion of Perforated Appendicitis

reverse
Start date: January 18, 2018
Phase: N/A
Study type: Interventional

A Prospective Randomized Controlled Trial of Reverse Conversion (Open to Laparoscopic) in management of Acute Perforated Appendicitis

NCT ID: NCT05145205 Completed - Clinical trials for Laparoscopic Surgery

Laparoscopic Sleeve Gastrectomy vs Laparoscopic Roux-en-Y Gastric Bypass

Start date: January 1, 2020
Phase:
Study type: Observational

This is a retrospective work on 200 morbid obese patients randomized and categorized into 2 groups according to the treatment method: the laparoscopic sleeve gastrectomy (LSG) and LRYGB groups, within the period from 2014 to 2019 and matched weight dissipation, complications, life quality, and negative events

NCT ID: NCT05121454 Completed - Clinical trials for Laparoscopic Surgery

Validation of Serenno CUO and IAP Measuring Device

Start date: November 15, 2021
Phase:
Study type: Observational

Serenno Medical Automatic Urine Output measuring device is intended to measure volumetric flow rate (total volume and rate) of urine produced per minute over long periods by a patient with a urinary catheter as well as high resolution IAP via bladder pressure (IBP). The device comprises a control unit located near the bed, and a disposable unit connected between the catheter and the urine collection tube/bag. The disposable unit is connected to the control unit with a tube. Frequent and accurate Intra-Abdominal Pressure measurements facilitate management of critical care patients, yet this parameter is normally measured manually, intermittently, and inaccurately. Automating IAP measurement will increase responsiveness, reduce workload, and potentially improve outcomes. The investigators goal is to validate the accuracy urinary catheter estimates of IAP compared to the gold standard during the application of a wide range of pressures controlled by a validated closed-loop insufflation reference. Primary Objective: The study objective is to evaluate the accuracy of the Serenno Medical IAP measurements in patients with indwelling urinary catheters vs. the gold standard - the Foley Manometer