NCT07046390

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
52

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Jul 2025

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress74%
Jul 2025Aug 2026

First Submitted

Initial submission to the registry

April 6, 2025

Completed
3 months until next milestone

First Posted

Study publicly available on registry

July 1, 2025

Completed
19 days until next milestone

Study Start

First participant enrolled

July 20, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 20, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 20, 2026

Last Updated

July 1, 2025

Status Verified

March 1, 2025

Enrollment Period

1 year

First QC Date

April 6, 2025

Last Update Submit

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 COMPARATOR

this group will receive triple injection peri-sartorius (TIPS) block. The block will be done after induction of general anesthesia before skin incision

Drug: nerve block with bupivacaine 0.25%Drug: No intervention

control group

NO INTERVENTION

control group will receive conventional analgesic regimen without having a regional block.

Interventions

0.25% bupivacaine

tips block group

No intervention

tips block group

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Location

MeSH Terms

Interventions

Nerve Block

Intervention Hierarchy (Ancestors)

Anesthesia, ConductionAnesthesiaAnesthesia and AnalgesiaDenervationNeurosurgical ProceduresSurgical Procedures, Operative

Central Study Contacts

abdelrahman mohammed hanafy, master

CONTACT

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

Locations