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Effect of distance between the femoral condyle and the Popliteal artery on needle placement in IPACK block on lower end of femur

The distance between the femoral condyle and the Popliteal artery: does it affects needle placement in IPACK block at the level of femoral condyles? An observational study - Nil

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/01/061234
Enrollment
60
Registered
2024-01-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M259- Joint disorder, unspecified

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Sancheti Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: This prospective observational study will be conducted after Ethics committee approval in the institute. Adult patients ( >18 years old) scheduled for unilateral total knee replacement surgery under subarachnoid block will be screened by the anesthesia team, and after successful screening, they were included in the study

Exclusion criteria

Exclusion criteria: hepatic or renal insufficiency, age 80 years old, patients undergoing general anesthesia, allergy or intolerance to one of the study medications, body mass index >40, diabetes mellitus, American Society of Anesthesiologists class IV, chronic gabapentin or pregabalin use (regular use for >3 months), chronic opioid use (taking opioids for >3 months, or daily oral morphine equivalent [OME] of >5 mg/d for 1 month), and patients with severe valgus deformity and flexion contracture

Design outcomes

Primary

MeasureTime frame
Distance between posterior of the knee capsule [PKC] and the popliteal artery [PA]Timepoint: at the time of the block

Secondary

MeasureTime frame
24 hours opioid consumptionTimepoint: 24 hours after surgery;Ability to move the footTimepoint: 6hrs and 24 hrs;Ability to perform physiotherapyTimepoint: 24 hours after the procedure;adequacy of LA spreadTimepoint: during block;Any procedure-related complications were recorded.Timepoint: after the procedure in recovery;Hemodynamic parameters and respiratory parametersTimepoint: preoperative period before blocks, after ACB and IPACK blocks and before induction of anesthesia, 60 min after extubation in the PACU, after 8 and 24 hours in the ward.;postoperative pain scores using VAS (0-10) and need for rescue analgesiaTimepoint: time 0 (immediate postoperative), 60 min, 8 hours and 24 hours

Countries

India

Contacts

Public ContactDr Sandeep Diwan

Sancheti Institute of orthopedics

sdiwan14@gmail.com9823029328

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026