Postoperative Pain Management in Cerebral Palsy - Comparative Observational Study"

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

130 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-02-15

Study Completion Date

2022-08-05

Brief Summary

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In this study, our aim is to examine orthopedic interventions, anesthesia method, postoperative pain level and management applied to patients with CP in biruni university hospital.

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Detailed Description

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Conditions

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Pain, Postoperative

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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regional block

epidural / peripheral nerve block

pain

Intervention Type BEHAVIORAL

postoperative pain

intravenous

intravenous analgesia

pain

Intervention Type BEHAVIORAL

postoperative pain

Interventions

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pain

postoperative pain

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Diagnosed with cerebral palsy between the ages of 3-15,
* Category 2 according to the Classification of the American Society of Anesthesiology (ASA 2),
* patients undergoing soft tissue release for knee or ankle flexion contracture of the lower extremity with palliative or reconstructive hip interventions

Exclusion Criteria

* Any child with CP younger than 3 years old and older than 15 years has undergone
* procedures without a specific diagnosis of CP,
* the need for bone surgery,
* requiring both hip, knee and ankle surgery in the same session,
* with autonomic neuropathy,
* Patients with a history of anticholinergic and vasoactive drug use or allergy to amide type local anesthetics

Minimum Eligible Age

3 Years

Maximum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No