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How Much is Too Much: Assessing Varying Pressure Pump Pressures in Post Operative Pain Control in Shoulder Arthroscopy.

How Much is Too Much: Assessing Varying Pressure Pump Pressures in Post Operative Pain Control in Shoulder Arthroscopy.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02896959
Enrollment
100
Registered
2016-09-12
Start date
2016-10-31
Completion date
Unknown
Last updated
2016-09-12

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

Conditions

Shoulder Arthroscopy

Brief summary

Postoperative surgical pain has been extensively study with regard to anaesthesia pain modalities, however little is published with regards to various arthroscopic shoulder surgical techniques. An intriguing characteristic of shoulder arthroscopy is the various arthroscopic pump pressures used by different surgeons. One could hypothesize that excessive water retention from the arthroscopic pump could causes excessive tissue pressure and swelling resulting in post operative pain. Unfortunately we could not find any literature in the English language regarding varying pressure pump settings on post operative pain control. For that reason we would like to assess how variable pump pressure effect tissue pressure over pre set time points, and how this may relate to post operative pain control.

Interventions

PROCEDUREArthroscopic rotator cuff repair

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients attending St. Joseph's hospital * Shoulder pathology amenable to arthroscopic surgery * Medically suitable for surgical management * Able to consent for surgery.

Exclusion criteria

* Unable to consent * Active infection * Active malignancy * Drug or alcohol misuse * Work related injury * Lack of permanent home residence * Previous surgery to affected shoulder * Medical contraindiction to surgery * Pregnant women

Design outcomes

Primary

MeasureTime frame
Pain - VAS scaleTwo years

Outcome results

None listed

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