- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04765579
Investigation of the Effect of 4 in 1 Block Application on Postoperative Analgesia in Knee Surgeries.
February 19, 2021 updated by: Seyran Köksal, Derince Training and Research Hospital
Effects of Ultrasonography-guided 4in1 Block Application on Postoperative Analgesia in Patients Undergoing Knee Surgery
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.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
62
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
knee surgeries performed with spinal anesthesia
Description
Inclusion Criteria:
- ASA I-II
- 18-60 ages
- who were informed about the study and accepted,
- who underwent knee surgery
Exclusion Criteria:
- ASA III-IV
- who are under general anesthesia
- who do not agree to participate in the study
- who are urgently operated
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
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
4in1
4in1 block will be applied in the operation room
|
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.
|
medical
medical analgesics will be applied in the service
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
visuel analogue scale
Time Frame: 6 months
|
0:No pain, 10:Very severe pain
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Anticipated)
February 20, 2021
Primary Completion (Anticipated)
July 20, 2021
Study Completion (Anticipated)
August 20, 2021
Study Registration Dates
First Submitted
February 16, 2021
First Submitted That Met QC Criteria
February 19, 2021
First Posted (Actual)
February 21, 2021
Study Record Updates
Last Update Posted (Actual)
February 21, 2021
Last Update Submitted That Met QC Criteria
February 19, 2021
Last Verified
February 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- Seyran-Tez
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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.
Clinical Trials on Visual Analogy Scala
-
Stanford UniversityNational Eye Institute (NEI)Enrolling by invitationRepetitive Transcranial Magnetic Stimulation | Visual Attention | Visual Cortical PlasticityUnited States
-
Brigham and Women's HospitalRecruitingIncidental Findings | Visual Attention | Visual Search | Hybrid SearchUnited States
-
Weill Medical College of Cornell UniversityCompletedIntraocular Pressure | Visual Acuity | Visual DisturbanceUnited States
-
University of TorontoKensington Eye InstituteTerminatedCataracts | Visual Acuity Reduced Transiently | Loss of Visual Contrast Sensitivity | Functional Visual LossCanada
-
Universitat Politècnica de CatalunyaNot yet recruiting
-
Johnson & Johnson Vision Care, Inc.Completed
-
Johnson & Johnson Vision Care, Inc.CompletedVisual AcuityUnited States
-
Johnson & Johnson Vision Care, Inc.Completed
-
Johnson & Johnson Vision Care, Inc.CompletedVisual AcuityUnited Kingdom
-
Johnson & Johnson Vision Care, Inc.CompletedVisual AcuityUnited States
Clinical Trials on visual analogy scala
-
University Hospital, GrenobleRecruiting
-
Samsun UniversityRecruitingPain CatastrophizingTurkey
-
Rigshospitalet, DenmarkNovo Nordisk A/SCompletedHematological Malignancy | GVHD, ChronicDenmark
-
Turku University HospitalUniversity of TurkuCompletedDepression | Sleep Disturbance | Prolonged PregnancyFinland
-
The University of Hong KongUnknownFall | Balance | Reinvestment Propensity | Gait RehabilitationHong Kong
-
Farmoquimica S.A.Unknown
-
Sakarya UniversityRecruitingNausea, Postoperative | Vomiting, Postoperative | Bariatric Surgical ProceduresTurkey
-
University of NebraskaTerminatedGait Disorders, NeurologicUnited States
-
Aveiro UniversityCompleted