ClinicalTrials.Veeva

Menu

Comparison of the Combination of Popliteal Sciatic and Femoral Block With the Combination of Ipack Adductor Canal Blocks (kneesurgery)

G

Gaziosmanpasa Research and Education Hospital

Status

Completed

Conditions

Early Mobility
Post-operative Analgesia

Treatments

Combination Product: combination femoral nerve and popliteal sciatica block
Combination Product: combination adductor canal and IPACK block

Study type

Observational

Funder types

Other

Identifiers

NCT06683313
knee surgeries blocks

Details and patient eligibility

About

Comparison of the combination of popliteal sciatic and femoral block with the combination of ipack adductor canal blocks and mobilization and analgesia duration in elective knee surgeries

Full description

There is concern that about half of patients with elective knee surgery report severe knee pain immediately after surgery. Optimal postoperative knee analgesia is important not only for patient comfort and satisfaction, but also to accelerate mobilization, functional recovery, and hospital discharge. To facilitate earlier ambulation and provide superior pain control, while striving for shorter hospital stays and same-day discharge for patients There is an increasing emphasis on multimodal analgesia and motor sparing regional anesthesia blocks.

To compare the postoperative analgesic efficacy of ipack adductor canal and femoral popliteal sciatic blocks in elective knee surgeries, and the first mobilization (bromage 0) times of motor block after spinal anesthesia. Our primary aim is to compare the ipack adductor canal block added after spinal anesthesia in elective knee surgeries with the combination of femoral + popliteal sciatic block. post of blocks To evaluate the operative mobilization (bromage 0) and analgesia times. Our secondary aims are to evaluate the first 4, 8, 12, 24 hours VAS (visual analog scale) values, first analgesia time, post op 1 hour bromage scores, postoperative nausea, vomiting, and discharge times, side effects. compare the incidence of effects.

Enrollment

93 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: knee operation,

Exclusion Criteria:Patients who did not consent to the procedure, those with coagulopathy, a known allergy to local anesthetics, a BMI > 35 kg/m², chronic analgesic and opioid use, mental or psychiatric disorders, or inability -

Trial design

93 participants in 2 patient groups

adductor canal block add ipack
Description:
Patients who received ipack add femoral canal block for postoperative analgesia
Treatment:
Combination Product: combination adductor canal and IPACK block
femoral block add popliteal sciatic
Description:
Patients who underwent popliteal sciatic block add femoral block for postoperative analgesia
Treatment:
Combination Product: combination femoral nerve and popliteal sciatica block

Trial contacts and locations

2

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems