- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07279805
Peripheral Perfusion Index as a Predictor of Post-spinal Hypotension in Patients Undergoing Lower Limb Surgeries
December 1, 2025 updated by: Ain Shams University
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 Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Cairo, Egypt
- Ain shams university
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
All patients undergoing elective lower limb surgeries at El-demerdash Hospital of Surgery during the study period.
Surgeries include Anterior/Posterior curciate ligament repair,knee arthroscopy,Hip and Knee replacement,tendon repair and varicose veins ligation.
Description
Inclusion Criteria:
Adult patients aging between 21-40 years of both sexes with average weight of 60-80 kg, and average height of 160-180.
- 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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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.
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Assess the ability of baseline peripheral perfusion index to predict post spinal hypotension
|
during the operation time.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 9, 2024
Primary Completion (Actual)
March 9, 2025
Study Completion (Actual)
March 9, 2025
Study Registration Dates
First Submitted
December 1, 2025
First Submitted That Met QC Criteria
December 1, 2025
First Posted (Actual)
December 12, 2025
Study Record Updates
Last Update Posted (Actual)
December 12, 2025
Last Update Submitted That Met QC Criteria
December 1, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- fmasu ms579/2024
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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