TIPS Block vs. IV Analgesia for Postoperative Pain After Knee Arthroscopy
Comparative Study Between Triple Injection Peri-Sartorius (TIPS) Block Versus Intravenous Analgesia for Postoperative Analgesia After Knee Arthroscopy
1 other identifier
interventional
52
1 country
1
Brief Summary
In this study participants are aiming to compare triple injection peri-sartorius (TIPS) block versus intravenous analgesia for postoperative analgesia after knee arthroscopy regarding efficacy of pain relief and early ambulation
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 6, 2025
CompletedFirst Posted
Study publicly available on registry
July 1, 2025
CompletedStudy Start
First participant enrolled
July 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 20, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 20, 2026
July 1, 2025
March 1, 2025
1 year
April 6, 2025
June 29, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
postoperative analgesics
24 hours postoperative
Secondary Outcomes (1)
The secondary outcomes will be the total morphine consumption in mg , ambulation distances during the first 24 hours postoperative in meters
24 hours postoperative
Study Arms (2)
tips block group
ACTIVE COMPARATORthis group will receive triple injection peri-sartorius (TIPS) block. The block will be done after induction of general anesthesia before skin incision
control group
NO INTERVENTIONcontrol group will receive conventional analgesic regimen without having a regional block.
Interventions
Eligibility Criteria
You may qualify if:
- Age 18-40 years undergoing knee arthroscopy. .Sex: Both sexes.
- American Society of Anaesthesiologists (ASA) Physical Status Class I and II
You may not qualify if:
- Declining to give written informed consent. .History of allergy to the medications used in the study. .Contraindications to regional anesthesia (including patient refusal, coagulopathy and local infection).
- Psychiatric disorder. .American Society of Anesthesiologists (ASA) Physical Status Class III and IV.
- Patients with body mass index (BMI) \>35 kg/m2 .Neurological deficits or mobility-related disorders of the non-operated limb .
- Moderate to severe hepatic , renal diseases and cardiac disease.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ain Shams University
Cairo, Egypt
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 6, 2025
First Posted
July 1, 2025
Study Start
July 20, 2025
Primary Completion (Estimated)
July 20, 2026
Study Completion (Estimated)
August 20, 2026
Last Updated
July 1, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share