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Adductor Canal Block Versus Patient Controlled Analgesia, in the Surgical Stress Response for Anterior Cruciate Ligament Repair

P

Pontificia Universidad Catolica de Chile

Status and phase

Withdrawn
Phase 1

Conditions

Surgery
Stress, Physiological
Anesthesia

Treatments

Device: Morphine Patient Controlled Analgesia
Procedure: Adductor Canal Block

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

To evaluate the surgical stress response in anterior cruciate ligament repair with an adductor canal block versus patient controlled endovenous analgesia.

Full description

Preoperative, 2 hours and 24 hours stress biomarkers will be evaluated in two groups of patients, continous adductor canal block and morphine patient controlled endovenous analgesia.

Sex

Male

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male,
  • 18-65 years,
  • traumatic Anterior Cruciate Ligament tear, scheduled for elective arthroscopic repair with Semitendinous-Gracillis technique at first time in the morning, with full articular range,
  • no other traumatologic lesions.

Exclusion criteria

  • denied consent to participate,
  • chronic steroids user,
  • diabetes type 1 or 2,
  • insulin resistance,
  • concurrent infectious disease,
  • cognitive failure, coagulopathy,
  • allergy to study drugs,
  • surgery scheduled in the afternoon

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Adductor Canal Block
Experimental group
Description:
With mild sedation, a continous bupivacaine 0.1% infusion catheter is placed in the adductor canal. Afterwards, patients are placed under General Anesthesia, and surgery starts. Preoperative, 2 hours and 24 hours stress biomarkers and analgesic quality will be measured.
Treatment:
Procedure: Adductor Canal Block
Patient Controlled Morphine Analgesia
Active Comparator group
Description:
Patients are placed under General Anesthesia, and after surgery, a Morphine patient controlled analgesia delivery system is installed. Preoperative, 2 hours and 24 hours stress biomarkers and analgesic quality will be measured.
Treatment:
Device: Morphine Patient Controlled Analgesia

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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