Endoscopy Clinical Trials

Clinical trials related to Endoscopy Procedure

Prospective Observational Cohort Study Comparing Recovery Profiles After Target-Controlled Infusion Versus Inhalational Anesthesia in Video-Assisted Thoracoscopic Surgery

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This study is designed as a prospective observational cohort to evaluate recovery after video-assisted thoracoscopic surgery (VATS). In our clinic, anesthesia for VATS is commonly provided either with target-controlled infusion (TCI) or with inhalational agents, depending on the routine practice of the anesthesiologist. No randomization or additional intervention will be performed. During the study period, patients who receive either method as part of standard care will be followed, and perioperative and postoperative data will be recorded. Awakening time, extubation time, Aldrete score progression, pain levels, and early postoperative complications will be compared between the two groups. The aim is to better understand how these widely used anesthesia techniques may influence recovery in VATS patients and to support future clinical decision-making.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Adults aged 18 to 65 years

⁃ Patients scheduled for elective video-assisted thoracoscopic surgery (VATS)

⁃ ASA physical status I-III

⁃ Able to provide informed consent

⁃ Planned postoperative recovery in PACU and surgical ward

Locations
Other Locations
Turkey
Istanbul University Cerrahpasa Medical Faculty
RECRUITING
Istanbul
Contact Information
Primary
mert katılmış, md
mertkatilmis97@gmail.com
+905346430560
Time Frame
Start Date: 2026-01-12
Estimated Completion Date: 2026-07
Participants
Target number of participants: 100
Treatments
TCI Group
Patients receiving target-controlled infusion (TCI) anesthesia as part of routine clinical care during VATS procedures. No intervention is assigned by the study team.
Inhalational Anesthesia Group
Patients receiving inhalational anesthesia (e.g., sevoflurane) as part of routine clinical care during VATS procedures. No intervention is assigned by the study team.
Related Therapeutic Areas
Sponsors
Leads: Istanbul University - Cerrahpasa

This content was sourced from clinicaltrials.gov