- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07700797
Adductor Canal Block With IPACK Versus 4-in-1 Block for Postoperative Analgesia in Knee Surgery
Effect of Adductor Canal Block With Infiltration of the Posterior Capsule of the Knee Versus 4-in-1 Block Technique for Postoperative Analgesia in Patients Undergoing Knee Surgeries
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Effective postoperative pain control following knee surgery is essential for early mobilization, rehabilitation, and patient satisfaction. Several regional anesthesia techniques have been developed to provide analgesia while preserving quadriceps muscle strength. Adductor Canal Block combined with Infiltration of the Posterior Capsule of the Knee (IPCAK) has been proposed as a motor-sparing technique that provides effective anterior and posterior knee analgesia. The 4-in-1 block is another ultrasound-guided regional anesthesia technique designed to provide comprehensive analgesia for knee surgery.
This prospective randomized interventional study enrolled 24 patients undergoing knee surgery. Participants were randomly assigned to receive either Adductor Canal Block with IPCAK or the 4-in-1 block. Postoperative pain scores, time to first rescue analgesia, total analgesic consumption, motor function, patient satisfaction, and complications were evaluated and compared between the two groups
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
Sharqia Province
-
Zagazig, Sharqia Province, Egypten, 055
- Faculty of Medicine, Zagazig University Hospitals
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
Tar emot friska volontärer
Beskrivning
Inclusion Criteria:
- 1. Patients or caregivers acceptance. 2. Age : 21 - 64 years 3. Sex : both ( males & females). 4. Physical status: ASA І & II. 5. BMI 18.5-30 kg/m2. 6. Type of operations : elective surgery. 7. Type of anesthesia: unilateral intrathecal anesthesia. 8. Patients undergoing elective knee surgery under unilateral spinal anesthesia 9. Duration of surgery within 2 hr.
Exclusion Criteria:
- Known history of allergy to study drug Coagulopathies or taking drugs affecting coagulation.. Contraindications for peripheral nerve block (PNB) and spinal anesthesia (SA) (coagulation defects, infection at the puncture site), bone degenerative disease and posttraumatic condition of the spine, dementia and severe visual or auditory disorder.
Current severe psychiatric disease, alcoholism or drug dependence. Subjects with history previous knee surgery, osteoarthritis, malformation or tumors (including Baker's cyst), which could alter the normal anatomy of the popliteal fossa
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Adductor canal block+ IPACK
Patients receive ultrasound-guided Adductor Canal Block combined with Infiltration of the Posterior Capsule of the Knee (IPCAK) for postoperative analgesia after knee surgery
|
Ultrasound-guided Adductor Canal Block combined with IPCAK block
|
|
Experimentell: 4 in 1 block
Patients receive ultrasound-guided 4-in-1 block for postoperative analgesia after knee surgery.
|
Ultrasound-guided 4-in-1 block technique.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Postoperative pain intensity measured by Visual Analog Scale (VAS)
Tidsram: 24 hours after surgery
|
Postoperative pain will be assessed using the Visual Analog Scale (VAS) at rest and during movement at predetermined postoperative time points
|
24 hours after surgery
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Total opioid consumption
Tidsram: First 24 hours after surgery
|
Total rescue opioid analgesic consumption during the first 24 postoperative hours
|
First 24 hours after surgery
|
|
Time to first rescue analgesia
Tidsram: Within 24 hours after surgery
|
Time from completion of surgery to the first request for rescue analgesia
|
Within 24 hours after surgery
|
|
Patient satisfaction with postoperative analgesia
Tidsram: 24 hours after surgery
|
Patient satisfaction score regarding postoperative pain management
|
24 hours after surgery
|
Samarbetspartners och utredare
Sponsor
Utredare
- Studiestol: Abdalla Mohamed Goda, MD, Faculty of medicine, Zagazig university
- Studierektor: Yasser Mohamed Naser, MD, Faculty of medicine, Zagazig university
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 1763
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
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