Clinical Trials Directory

Trials / Completed

CompletedNCT02967640

Does Subacromial Injection With Glutamate Receptor Antagonist, Ketamine, Attenuate Pain in Rotator Cuff Tendinopathy?

Does Subacromial Injection With Glutamate Receptor (NMDAR) Antagonist, Ketamine, Attenuate Pain in Rotator Cuff Tendinopathy?

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
14 (actual)
Sponsor
Helse Møre og Romsdal HF · Other Government
Sex
All
Age
40 Years
Healthy volunteers
Not accepted

Summary

The hypothesis of the present study is that in patients with rotator cuff tendinopathy a specific pharmacological blocking of peripheral glutamate-receptor N-methyl-d-aspartate receptor type1 (NMDAR) glutamate receptors will result in pain alleviation. Activated NMDAR1 has been demonstrated to be crucial for pain regulation in various pain disorders, and in biopsies from patients with tendinopathy, NMDAR1 was found to be activated. To test this hypothesis a specific NMDA receptor antagonist, ketalar (ketamine), will be injected guided by ultrasound into the subacromial space in patients with rotator cuff tendinopathy, and subsequently the pain response will be assessed.

Conditions

Interventions

TypeNameDescription
DRUGKetalar2,5 ml - if well tolerated immediately followed by another 2,5 ml - of an approximately 1 mg/ml ketalar solution (1 ml of ketalar 10 mg/ml + 9 ml of NaCl 9%) injected 2 times with 1-12 weeks between each injection
DRUGNaCl 9%2,5 ml - if well tolerated immediately followed by another 2,5 ml - of a 9% NaCl solution injected 2 times with 1-12 weeks between each injection

Timeline

Start date
2018-05-30
Primary completion
2024-12-30
Completion
2024-12-30
First posted
2016-11-18
Last updated
2025-08-22

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT02967640. Inclusion in this directory is not an endorsement.