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Open Surgery clinical trials

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NCT ID: NCT06219993 Active, not recruiting - Biliary Atresia Clinical Trials

Robot-assisted Modified Kasai Portoenterostomy Versus Open Kasai Portoenterostomy for Biliary Atresia

RKPEVSOKPE
Start date: December 21, 2023
Phase:
Study type: Observational [Patient Registry]

Open Kasai portoenterostomy (OKPE) is considered the standard treatment procedure for biliary atresia (BA). Robotic-assisted Kasai portoenterostomy (RAKPE) has been utilized to treat BA. However, there were no randomized controlled trials to verify its effectiveness. The objection was to compare the efficacy of Da Vinci robot-assisted with open Kasai portoenterostomy for biliary atresia.

NCT ID: NCT05019404 Recruiting - Clinical trials for Minimally Invasive Surgery

Minimally Invasive Surgical Epilepsy Trial for Temporal Lobe Epilepsy

MISET-TLE
Start date: April 25, 2023
Phase: N/A
Study type: Interventional

Temporal lobe epilepsy (TLE) is a chronically neurological disease characterized by progressive seizures. TLE is the most frequent subtype of refractory focal epilepsy in adults. Epilepsy surgery has proven to be very efficient in TLE and superior to medical therapy in two randomized controlled trials. According to the previous experience, the investigators use functional anterior temporal lobectomy (FATL) via minicraniotomy for TLE. To date, this minimally invasive open surgery has been not reported. The investigators here present a protocol of a prospective trail which for the first time evaluates the outcomes of this new surgical therapy for TLE.

NCT ID: NCT04843436 Recruiting - Open Surgery Clinical Trials

PRIMO Post-Market Clinical Follow Up Study

PRIMO
Start date: April 13, 2021
Phase: N/A
Study type: Interventional

Post Market Clinical Follow up Study aimed to collect clinical data on safety and efficacy of Robotically Assisted System called Symani to perform microsurgery techniques such as anastomosis, suturing and ligation for open surgery procedures on small anatomical structures such as blood vessels, lymphatic ducts and nerves.

NCT ID: NCT01596049 Terminated - Open Surgery Clinical Trials

The Efficacy of a Self-fixating Mesh in Unilateral Open Inguinal Hernia Repair

Start date: May 2012
Phase: N/A
Study type: Observational

This study's objective is to assess the efficacy of a Self-fixating mesh in the surgical repair of unilateral inguinal hernia, which is becoming the new standard of care in open surgical repair of inguinal hernia. The study design is interventional, enrolling 300 patients above 18 years of age, admitted for elective repair in the surgical department of Rambam Medical Health Care Campus, an academic medical center. The study will assess several outcomes including post-surgical pain, recurrence, quality of life and post surgical complications (e.g. wound infection, the formation of hematoma or seroma, etc).