Skip to content

Evaluation of Postoperative Pain Following Bascom Cleft Lift Operation

Evaluation of Post-operative Pain in Bascom Cleft Lift Operation Receiving Multimodal Analgesia and Spinal Saddle Block in Day Case Surgery Setting.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02196727
Enrollment
32
Registered
2014-07-22
Start date
2013-05-31
Completion date
2014-04-30
Last updated
2014-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Keywords

Postoperative pain, Multimodal analgesia, Bascom Cleft Lift, Day-case.

Brief summary

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.

Interventions

None listed

Sponsors

Hvidovre University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Numerical Rating Scale (NRS) pain score (0=no pain, 10= maximum imaginable pain)24 hours postoperatively

Secondary

MeasureTime frame
Numerical Rating Scale (NRS) pain score (0=no pain, 10= maximum imaginable pain)2 hours, 48 hours and 30 days postoperatively

Other

MeasureTime frameDescription
Returning to leisure activities30 daysQuestionnaire: Yes or No
Nausea2 hours postoperativelyScale (0= non, 1= mild, 2= moderate, 3= severe)
Vomiting2 hours postoperativelyScale (0= non, 1= mild, 2= moderate, 3= severe)
Wound condition30 daysWound inspection for healing problems or infection
Returning to work30 daysQuestionnaire: Yes or No

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026