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Pain Control After Orthognathic Surgery (PCOGS)

Primary Purpose

Postoperative Pain

Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Trigeminal nerve block
Trigeminal nerve block
Trigeminal nerve block
Sponsored by
Chang Gung Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postoperative Pain focused on measuring Orthognathic surgery, Pain control, Trigeminal nerve, Levobupivacaine

Eligibility Criteria

20 Years - 40 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • all patients who will receive orthognathic surgery (one jaw or two jaw, with or without genioplasty) in Chang Gung Memorial Hospital since July 2011

Exclusion Criteria:

  • more complex (2- or more piece LeFort I osteotomy, combined gonial resection in BSSO, etc.) or less complex (only Wassmund and/or Kole osteotomies in upper or lower jaw) orthognathic procedures
  • unexpected fracture (unilateral)
  • intra-operative nerve injuries
  • significant facial asymmetry which demands different procedures (location of osteotomy, extension of muscle stripping, etc.)
  • cleft patient, post-traumatic patients, patients with craniofacial syndromes or other neurological or systemic problems which might interfere pain evaluation post-operatively

Sites / Locations

  • Chang Gung Memorial HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

Experimental

Arm Label

5ml 5% levobupivacaine

5ml normal saline

2.5ml 5% levobupivacaine

Arm Description

5ml 5% levobupivacaine to both maxillary and mandibular branches of trigeminal nerve on experimental side. (total 10ml)

5ml for maxillary and mandibular branches of trigeminal nerve (total 10ml on controlled side)

2.5ml 5% levobupivacaine to both maxillary and mandibular branches of trigeminal nerve on experimental side. (total 10ml)

Outcomes

Primary Outcome Measures

Postoperative pain
The degree of pain will be measured daily by visual analog scale.

Secondary Outcome Measures

Effective duration of levobupivacaine nerve block

Full Information

First Posted
August 12, 2011
Last Updated
September 4, 2011
Sponsor
Chang Gung Memorial Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01418183
Brief Title
Pain Control After Orthognathic Surgery
Acronym
PCOGS
Official Title
Intra-operative Trigeminal Nerve Block For Post-operative Pain Control After Orthognathic Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
June 2011
Overall Recruitment Status
Unknown status
Study Start Date
July 2011 (undefined)
Primary Completion Date
June 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chang Gung Memorial Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will assess the efficacy and safety of levobupivacaine for postoperative pain control in patients received orthognathic surgery. In this split-mouth study, each side will be randomized to receive 1) 5ml 0.5% levobupivacine, 2) 2.5ml 0.5% levobupivacaine, or 3) placebo. One shot of these agents will be delivered by nerve block to maxillary and mandibular branches of trigeminal nerve before the incision was made. The degree of postoperative pain will be evaluated daily by visual analog scale for up to 3 days. The anticipated time on study is 1 year, and the target sample size is 40 individuals.
Detailed Description
Design of intervention vs. control Intra-operative injective of (chirocaine) before incision Location of injection: inferior alveolar nerve proximal to its entrance to ramus of mandible, maxillary nerve around pterygopalatine ganglion Amount of injection on each injection site: (1) Experimental group 1: 5mg/ml chirocaine 5cc (2)Experimental group 2: 5mg/ml chirocaine 2.5cc (3)Control group: normal saline 5cc. There are totally 4 injection sites for two jaw surgery and 2 injection sites for one jaw surgery. The experimental site and control site will be determined randomly before injection. Outcome measurement Primary: effectiveness of intra-operative nerve block on post-operative pain control Secondary: whether the pain relieve effect is dose-related how long will this effect last The intensity of post-operative pain will be measured by VAS, visual analog scale)daily until patients are discharged. Report adverse outcome: Intolerable pain on control group Adverse reaction to local anesthetic agent Injection-related complications (puncture of major vessels, hematoma on -injection site, etc.)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Pain
Keywords
Orthognathic surgery, Pain control, Trigeminal nerve, Levobupivacaine

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
5ml 5% levobupivacaine
Arm Type
Experimental
Arm Description
5ml 5% levobupivacaine to both maxillary and mandibular branches of trigeminal nerve on experimental side. (total 10ml)
Arm Title
5ml normal saline
Arm Type
Placebo Comparator
Arm Description
5ml for maxillary and mandibular branches of trigeminal nerve (total 10ml on controlled side)
Arm Title
2.5ml 5% levobupivacaine
Arm Type
Experimental
Arm Description
2.5ml 5% levobupivacaine to both maxillary and mandibular branches of trigeminal nerve on experimental side. (total 10ml)
Intervention Type
Procedure
Intervention Name(s)
Trigeminal nerve block
Other Intervention Name(s)
5ml Chirocaine
Intervention Description
5ml of long-effective local analgesics (5% levobupivacaine) will be delivered to maxillary and mandibular branches of trigeminal nerve.
Intervention Type
Procedure
Intervention Name(s)
Trigeminal nerve block
Other Intervention Name(s)
2.5ml Chirocaine
Intervention Description
2.5ml of long-effective local analgesics (5% levobupivacaine) will be delivered to maxillary and mandibular branches of trigeminal nerve.
Intervention Type
Procedure
Intervention Name(s)
Trigeminal nerve block
Other Intervention Name(s)
Placebo
Intervention Description
5ml Normal saline will be delivered to maxillary and mandibular branches of trigeminal nerve.
Primary Outcome Measure Information:
Title
Postoperative pain
Description
The degree of pain will be measured daily by visual analog scale.
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 3days
Secondary Outcome Measure Information:
Title
Effective duration of levobupivacaine nerve block
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 3 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: all patients who will receive orthognathic surgery (one jaw or two jaw, with or without genioplasty) in Chang Gung Memorial Hospital since July 2011 Exclusion Criteria: more complex (2- or more piece LeFort I osteotomy, combined gonial resection in BSSO, etc.) or less complex (only Wassmund and/or Kole osteotomies in upper or lower jaw) orthognathic procedures unexpected fracture (unilateral) intra-operative nerve injuries significant facial asymmetry which demands different procedures (location of osteotomy, extension of muscle stripping, etc.) cleft patient, post-traumatic patients, patients with craniofacial syndromes or other neurological or systemic problems which might interfere pain evaluation post-operatively
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yi-Chieh Chen, MD
Phone
+886-975-365553
Email
Pschenyc@yahoo.com.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yi-Chieh Chen, MD
Organizational Affiliation
Chang Gung Memorial Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chang Gung Memorial Hospital
City
Taipei
ZIP/Postal Code
10507
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yi-Chieh Chen, MD
Email
Pschenyc@yahoo.com.tw
First Name & Middle Initial & Last Name & Degree
Yi-Chieh Chen, MD

12. IPD Sharing Statement

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Pain Control After Orthognathic Surgery

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