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Clinical Trials/NCT05946850
NCT05946850RecruitingNot Applicable

Caudal Analgesia in Anticoagulated Chronic Pain Patients

Salem Anaesthesia Pain Clinic1 site in 1 country100 target enrollmentStarted: January 2, 2008Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
Pain score, objective measurement using the validated Numeric Pain Rating scale

Study Overview

Brief Summary

Caudal analgesia is an effective intervention for lumbosacral pain. Some chronic pain patients take anticoagulants for vasculopathy treatment. Anticoagulation limits the use of caudal analgesia because of the risk of epidural bleeding. Caudal analgesia may be safe and effective in anticoagulated chronic pain patients.

Quantitative analysis of prospective clinical data. Evaluation of caudal analgesia efficacy and safety in anticoagulated chronic pain patients. Analysis of outcome, and complications.

Detailed Description

Caudal analgesia is an effective interventional therapy for chronic lumbosacral pain. Some chronic pain patients take anticoagulants for vasculopathy treatment. Anticoagulation limits the use of caudal analgesia because of the risk of epidural bleeding. Anticoagulation may be discontinued briefly, to allow caudal injection. Interruption of anticoagulation may be difficult and dangerous for some high-risk patients. Caudal analgesia may be safe and effective in anticoagulated chronic pain patients.

Quantitative analysis of prospective clinical data. An evaluation of caudal analgesia safety in anticoagulated chronic pain patients. An analysis of treatment outcome, and complications.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
20 Years to 99 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •adult chronic pain patients who undergo caudal analgesia

Exclusion Criteria

  • •chronic pain patients who refuse caudal analgesia

Outcomes

Primary Outcomes

Pain score, objective measurement using the validated Numeric Pain Rating scale

Time Frame: 12 weeks

Pain score, using the Numeric Pain Rating scale of 0 to 10, low scores indicate less pain, high scores indicate worse pain

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Salem Anaesthesia Pain Clinic
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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