Chronic Pain Syndrome Clinical Trial
Official title:
Peripheral Nerve Field Stimulation by Thermal Micro-cautery for Painful Knee Osteoarthritis: Non Randomised Controlled Trial
To trial a traditional pain management technique from Ayurveda in a modern way - the technique involves micro - cautery to painful areas in knee osteoarthritis for patients on a waiting list for knee replacement. The Investigators will include a waiting list control series.
The Research and Ethics Committee at Tallaght University Hospital approved the recruitment of
patient into the study by invitation. Patients who accepted the invitation were enrolled into
the intervention group and patients who declined the invitation were enrolled into the
control group and both groups were followed up for 8 week period. Agnikarma is a traditional
surgical technique (thermal cautery) described in ancient surgical manuscripts for the
treatment of severe persistent pain.
It applies intense heat to points of maximum pain agreed with the patient pre procedure. The
heat is applied by a metal rod (Shalaka) heated in an open naked flame. The rod is applied to
the skin at the agreed pain point in an even manner and generates a micro second degree burn.
A traditional herbal cream is then applied which cools the application as reported by the
patient. It is usual to allow skin healing to occur before the application of further heat
(1-2 weeks). The pain points can move within a painful area and the technique best works with
precise application to the current pain point. So before each application the precise points
are agreed with the patient in advance by demarcating the painful area with a pen and
searching for the points of maximum tenderness within that field.
The purpose of this study was simply to define if indeed this technique delivers pain relief
as observed in practice. The investigators chose one group to study - painful knee arthritis.
In this condition patients often wait many years for the definitive procedure and run some
risks with current pain relief treatment. As these patients were not the normal attendees at
a pain clinic the investigators decided in advance to limit the study to 4 applications over
a 4- 8 week period, the latter to allow for different speeds at which the skin might heal.
The investigators recruited both our interventional group and waiting list control group from
the same orthopedic waiting list.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT01417923 -
The Immune and Clinical Impacts of Vitamin D in Patients With Chronic Musculo-skeletal Pain
|
Phase 4 | |
Completed |
NCT03472521 -
Prevention of Persistent Opioid Use in Mothers
|
Phase 4 | |
Not yet recruiting |
NCT03249025 -
Lidocaine-Ketamine for Management of Chronic Pain
|
N/A | |
Enrolling by invitation |
NCT06359561 -
Assessment of Effectiveness and Stimulation Coverage of Closed-loop Spinal Cord Stimulation (CL-SCS) Therapy in Patients With Cervical Lead Placement
|
||
Recruiting |
NCT05877274 -
Sodium Channel Mutations in Patient With the Anterior Cutaneous Nerve Entrapment Syndrome (ACNES)
|
||
Completed |
NCT03317782 -
NoL Index Variations Before and After a Stellate Ganglion Block
|
||
Completed |
NCT04199858 -
Electrophysiological Correlates of Nocebo Effects on Pain
|
N/A | |
Recruiting |
NCT05491499 -
Assessing the Impact of Exercise Based Intensive Interdisciplinary Pain Treatment (IIPT) on Endogenous Pain Modulation in Youth With Chronic Pain Syndromes
|
||
Active, not recruiting |
NCT05090683 -
Evaluation of a Mind-body Based Application for the Treatment of Chronic/Persistent Pain.
|
N/A | |
Completed |
NCT04197154 -
Pain-related Fear as a Facilitator of Nocebo Hyperalgesia
|
N/A | |
Completed |
NCT04209764 -
Prevalence of Pain in the Departments of Surgery and Oncoematology of a Children's Hospital
|
||
Recruiting |
NCT06071962 -
Long Term Efficacy and Tolerability of AP707 in Patients With Chronic Back Pain
|
Phase 3 | |
Recruiting |
NCT06072001 -
Long Term Efficacy and Tolerability of AP707 in Patients With Chronic Pain Due to Central Neuropathy of Any Genesis
|
Phase 3 | |
Recruiting |
NCT06071949 -
Efficacy and Tolerability of AP707 in Patients With Chronic Pain Due to Central Neuropathy of Any Genesis
|
Phase 3 | |
Recruiting |
NCT06071988 -
Long Term Efficacy and Tolerability of AP707 in Patients With Chronic Pain Due to Traumatic or Post-operative Peripheral Neuropathy
|
Phase 3 | |
Recruiting |
NCT06072560 -
Efficacy and Tolerability of AP707 in Patients With Chronic Back Pain
|
Phase 3 | |
Recruiting |
NCT06072573 -
Efficacy and Tolerability of AP707 in Patients With Chronic Pain Due to Diabetic Polyneuropathy
|
Phase 3 | |
Recruiting |
NCT06071975 -
Long Term Efficacy and Tolerability of AP707 in Patients With Chronic Pain Due to Diabetic Polyneuropathy
|
Phase 3 | |
Recruiting |
NCT06071936 -
Efficacy and Tolerability of AP707 in Patients With Chronic Pain Due to Traumatic or Post-operative Peripheral Neuropathy
|
Phase 3 | |
Recruiting |
NCT05678127 -
A Pilot Study to Explore the Use of Skin Biopsy as Diagnostic Tool in Anterior Cutaneous Nerve Entrapment Syndrome (ACNES)
|
N/A |