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Clinical Trials/NCT07279805
NCT07279805
Completed
Not Applicable

Peripheral Perfusion Index as a Predictor of Post-spinal Hypotension in Patients Undergoing Lower Limb Surgeries

Ain Shams University1 site in 1 country40 target enrollmentStarted: September 9, 2024Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
Assess the ability of baseline peripheral perfusion index to predict post spinal hypotension spinal anesthesia-induced hypotension in patients undergoing lower limb surgeries

Overview

Brief Summary

This prospective observational study was carried out on a sample of 40 patients over a period of 6 months to asses the peripheral perfusion index as a Predictor for post spinal hypotension in patient undergoing lower limp surgeries.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
21 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Adult patients aging between 21-40 years of both sexes with average weight of 60-80 kg, and average height of 160-
  • Patients undergoing Elective Lower limb Surgeries under successful spinal anesthesia (duration of surgery 45-120 minutes).
  • ASA physical status classes I - II.

Exclusion Criteria

  • Patient's refusal of procedure or participation in the study.
  • ASA classes III or above. Coagulopathy and bleeding disorders.
  • Body mass index \>40kg/m2
  • Contraindications to spinal anesthesia.
  • Hypersensitivity to the study medications.
  • Patients receiving vasoactive drugs.
  • Patients undergoing emergency surgery.
  • Duration more than 2hours.
  • Major bleeding.

Outcomes

Primary Outcomes

Assess the ability of baseline peripheral perfusion index to predict post spinal hypotension spinal anesthesia-induced hypotension in patients undergoing lower limb surgeries

Time Frame: during the operation time.

Assess the ability of baseline peripheral perfusion index to predict post spinal hypotension

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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