MedTrace Logo

Popliteal Block for Postoperative Pain in Knee-ankle Soft Tissue Surgery in Cerebral Palsy

NCT02507700 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2016-06-13

No results posted yet for this study

Summary

Popliteal block is a technique for providing postoperative pain management in children. In this randomized double-blinded study, the investigators evaluated the effects of preoperative popliteal nerve block on postoperative pain and analgesic requirement in children with cerebral palsy (CP) undergoing knee-anckle soft tissue surgery. The Wong Baker faces scale and skin conductance fluctuations will be assessed.

Conditions

  • Postoperative Pain
  • Cerebral Palsy

Interventions

PROCEDURE

Popliteal block

In group P, popliteal block will be performed with ultrasound guidence.

DRUG

Sevoflurane

Sevoflurane will be used to all patient's for anesthesia induction and maintenance

DEVICE

Ultrasound

For recognize the nerve (sciatic nerve), ultrasound will be used in group P.

OTHER

Plaster cover

Plaster cover will be used to control group for sham procedure

DRUG

bupivacaine

Bupivacaine 0.25% will be performed for popliteal block to group P.

OTHER

Laryngeal mask airway

After anesthesia induction, laryngeal mask airway will be inserted to all patients

Sponsors & Collaborators

  • Diskapi Teaching and Research Hospital

    lead OTHER

Principal Investigators

  • Taylan Akkaya · Ministry of Health Diskapi Yıldırım Beyazıt Training and Research Hospital

  • Mesut Bakır · Ministry of Health Diskapi Yıldırım Beyazıt Training and Research Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
3 Years
Max Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2016-05-31
Completion
2016-06-30

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02507700 on ClinicalTrials.gov