Investigation of the Effect of 4 in 1 Block Application on Postoperative Analgesia in Knee Surgeries.
Effects of Ultrasonography-guided 4in1 Block Application on Postoperative Analgesia in Patients Undergoing Knee Surgery
1 other identifier
observational
62
0 countries
N/A
Brief Summary
to investigate the effects of ultrasonography-guided 4in1 block application on postoperative analgesia in patients undergoing knee surgery. After knee surgeries performed with spinal anesthesia, 4in1 block will be applied in one group and medical analgesics will be applied in the service in the other group.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Feb 2021
Shorter than P25 for all trials
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
February 16, 2021
CompletedStudy Start
First participant enrolled
February 20, 2021
CompletedFirst Posted
Study publicly available on registry
February 21, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 20, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
August 20, 2021
CompletedFebruary 21, 2021
February 1, 2021
5 months
February 16, 2021
February 19, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
visuel analogue scale
0:No pain, 10:Very severe pain
6 months
Study Arms (2)
4in1
4in1 block will be applied in the operation room
medical
medical analgesics will be applied in the service
Interventions
We will investigate the effect of 4in1 block by questioning the vas score of the patients, its effect on quadriceps strength, and additional analgesia needs for 24 hours.
Eligibility Criteria
knee surgeries performed with spinal anesthesia
You may qualify if:
- ASA I-II
- ages
- who were informed about the study and accepted,
- who underwent knee surgery
You may not qualify if:
- ASA III-IV
- who are under general anesthesia
- who do not agree to participate in the study
- who are urgently operated
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- resident
Study Record Dates
First Submitted
February 16, 2021
First Posted
February 21, 2021
Study Start
February 20, 2021
Primary Completion
July 20, 2021
Study Completion
August 20, 2021
Last Updated
February 21, 2021
Record last verified: 2021-02
Data Sharing
- IPD Sharing
- Will not share