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Effects of Anesthesia Techniques on Tissue Oxygenation and Recovery in Lower Abdominal Surgery

A Prospective Observational Study on the Effects of Anesthesia Techniques on Tissue Oxygenation and Postoperative Recovery in Lower Abdominal Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07102108
Enrollment
180
Registered
2025-08-03
Start date
2023-03-01
Completion date
2025-03-01
Last updated
2025-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lower Abdominal Surgery

Brief summary

This is a prospective observational study designed to evaluate the effects of different anesthesia techniques on tissue oxygenation and postoperative recovery in patients undergoing lower abdominal surgery. A total of 180 patients will be enrolled and evenly allocated into four groups based on the anesthesia method used: general anesthesia, spinal anesthesia, epidural anesthesia, and combined general plus epidural anesthesia. Near-infrared spectroscopy (NIRS) will be utilised to monitor tissue oxygenation at the thenar and plantar regions during the perioperative period. Vital signs, VAS scores(min 0-max 10 points), Quality of Recovery-40 (QoR-40) scores(min 40-max 200 points), and additional postoperative recovery parameters- including length of stay in the post-anesthesia care unit and hospital, surgical site infection, wound revision, and mortality- will be recorded and compared across the groups. The primary hypothesis is that regional anesthesia techniques enchance tissue oxygenation and are associated with improved postoperative recovery outcomes compared to general anesthesia alone. The study was approved by the local ethics committee and will be conducted at a single tertiary-care center.

Interventions

None listed

Sponsors

Trakya University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Days to 80 Days
Healthy volunteers
No

Inclusion criteria

* Adults aged 18-80 years * Scheduled for elective lower abdominal surgery * Eligible for general, spinal, epidural or combined anesthesia techniques * Provided writen informed consent * ASA physical status 1-3

Exclusion criteria

* Refusal to participate * Emergency surgery * Severe cardiovascular or respiratory instability * Pre-existing severe cognitive impairment of communication barrier * Peripheral vascular disease affecting NIRS readind * Local infection or anatomical anomaly preventing regional anesthesia

Design outcomes

Primary

MeasureTime frameDescription
Tissue Oxygenation Levels Measured by NIRSFrom baseline(pre-op) to end of surgeryContinuous measurement of tissue oxygenation at thenar and plantar sites using near-infrared spectroscopy during perioperative period

Secondary

MeasureTime frameDescription
Intraoperative Vital SignsIntraoperative periodSystolic blood pressure recorded during anesthesia
Visual Analog Scale(VAS) Pain ScoresUp to 24 hours after surgeryVAS pain scores measured postoperatively at PACU and postoperative day 1. The scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst possible pain. Higher scores indicate worse outcomes.
Qor-40 Questionnaire Scorespostoperative day 1Quality of Recovery scores assessed using the Qor-40 questionnaire on postoperative day1. The total score ranges from 40 to 200, with higher scores indicating better recovery.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026