Evaluation of Postoperative Pain Following Bascom Cleft Lift Operation

NCT ID: NCT02196727

Last Updated: 2014-07-22

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

COMPLETED

Total Enrollment

32 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-05-31

Study Completion Date

2014-04-30

Brief Summary

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The purpose of this study is to evaluate postoperative pain in Bascom Cleft Lift operation receiving multimodal analgesia in day-case surgery setting.

Hypothesis: Multimodal analgesia provides adequate pain relief in patients undergoing Bascom Cleft Lift operation.

Detailed Description

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Conditions

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Postoperative Pain

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients undergoing Bascom operation

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Age \> 18
* ASA physical status 1 and 2
* Patient undergoing Bascom operation in prone position

Exclusion Criteria

* Pregnancy
* Current regular use of drug belonging to the class of opioids
* Allergy/ intolerance to drugs included in multimodal analgesia regime
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hvidovre University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Saphana Jassim Mohamed

Consultant

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hvidovre Univarsity Hospital

Hvidovre, Copenhagen, Denmark

Site Status

Countries

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Denmark

References

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Mohamed SJ, Kristensen BB, Lindgaard L, Bisgaard T. Acceptable effect of multimodal analgesic treatment after a Bascom cleft lift operation. Dan Med J. 2015 Jan;62(1):A4985.

Reference Type DERIVED
PMID: 25557329 (View on PubMed)

Other Identifiers

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BPP

Identifier Type: -

Identifier Source: org_study_id

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