Peripheral Nerve Block (Femoral - Sciatic - Obturator) Versus General Anesthesia for Arthroscopic ACL Repair

NCT ID: NCT02186899

Last Updated: 2014-07-10

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

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-03-31

Study Completion Date

2015-12-31

Brief Summary

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Arthroscopic ACL repair can be performed under different types of anesthesia. In the last few years peripheral nerve blocks have increased their popularity for this kind of operation. The investigators want to see how the type of anesthesia and postoperative analgesia effects the time required for patient mobilisation.

Detailed Description

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Conditions

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Arthroscopic ACL Rerpair Surgery Anesthesia Care

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors

Study Groups

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General Anesthesia Femoral continuous

General anesthesia plus continuous femoral nerve block

Group Type ACTIVE_COMPARATOR

General anesthesia femoral continuous

Intervention Type OTHER

General anesthesia Femoral bolus

General anesthesia plus single shot femoral nerve block

Group Type ACTIVE_COMPARATOR

General Anesthesia femoral bolus

Intervention Type OTHER

Femoral Sciatic Obturator Nerve block

Ultrasound guided femoral plus sciatic plus obturator nerve block

Group Type ACTIVE_COMPARATOR

Ultrasound Guided Femoral Sciatic Obturator nerve blocks

Intervention Type OTHER

Interventions

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Ultrasound Guided Femoral Sciatic Obturator nerve blocks

Intervention Type OTHER

General Anesthesia femoral bolus

Intervention Type OTHER

General anesthesia femoral continuous

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age 18 - 80 yrs
* ASA I - III
* ACL surgery

Exclusion Criteria

* Coagulopathy disorders
* Infection at the puncture site for the interscalene block
* Neurologic deficit in the arm that is going to be operated
* Allergy to local anesthetics
* BMI \> 35
* Psychiatric disorders
* Patient's refusal
* Problems with patient communication
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Larissa University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Marina Simaioforidou

Anesthesiologist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Marina Simaioforidou, Medicine

Role: STUDY_DIRECTOR

Private Clinic of Larissa "Asklipeiio"

George Basdekis, Medicine

Role: STUDY_CHAIR

Private Clinic of Larissa "Asklipeiio"

Konstantinos Bargiotas, Medicine

Role: STUDY_CHAIR

Larissa University Hospital

Aristeidis Zibis, Medicine

Role: STUDY_CHAIR

Private Clinic of Larissa "Askipeiio"

Athanasios Drakos, Medicine

Role: STUDY_CHAIR

Larissa University Hospital

Metaxia Bareka, Medicine

Role: PRINCIPAL_INVESTIGATOR

Larissa University Hospital

Locations

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Private Clinic of Larissa "Asklipeiio"

Larissa, Larissa, Greece

Site Status RECRUITING

Countries

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Greece

Central Contacts

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Marina Simaioforidou, Medicine

Role: CONTACT

00306947845083

Facility Contacts

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Marina Simaioforidou, Medicine

Role: primary

Other Identifiers

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FSOvsGA

Identifier Type: -

Identifier Source: org_study_id

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