Overview
Dexmedetomidine, Ozone and Dexamethasone Local Injection in Carpal Tunnel Syndrome for Pain Relief
Status:
Recruiting
Recruiting
Trial end date:
2024-11-01
2024-11-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The aim of the present study is to compare the analgesic efficacy of Dexmedetomidine, Ozone and Dexamethasone regional injection in carpal tunnel syndrome.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Tanta UniversityTreatments:
Dexamethasone
Dexmedetomidine
Criteria
Inclusion Criteria:- Age from 20 to 60 years.
- Both sexes.
- Patients with ultrasonographic evidence of mild-to-moderate carpal tunnel syndrome
(CTS).
- Inclusion criteria will include numbness and pain in the median nerve (MN)
distribution persisting for minimum of 3 months , nerve conduction studies (NCS)
consistent with carpal tunnel syndrome (CTS) as per the American Association of
Neuromuscular and Electro diagnostic Medicine (AANEM) guidelines, and an median nerve
(MN) cross-sectional area (CSA)at the wrist >12 mm2 suggesting mild-to-moderate CTS
forms.
Exclusion Criteria:
- Patient refusal.
- Patients with severe symptoms and signs of CTS as identified per the American
Association of Neuromuscular and Electro diagnostic Medicine (AANEM) guidelines,[14]
as this is an indication for surgery,
- Patients who show improvement on medical treatment,
- Previous surgical or injectional CTS treatment,
- Pregnancy ,co existence of brachial plexopathy, or thoracic outlet syndrome,
polyneuropathy, radiculopathy and peripheral nerve lesion in upper limb.
- Severe cardiovascular disease
- Morbid obese patients (body mass index (BMI) of >35 kg/m2)
- Infection at site of injection.
- Bleeding diathesis.
- History of thyroid deficiency, uncontrolled diabetes mellitus , rheumatoid arthritis
and history of glucose-6-phosphate dehydrogenase (G6PD) deficiency
- History of Ozone or Dexmedetomidine allergy.
- End stage renal and hepatic disease.
- History of inflammatory joint , connective tissue disorders, , burns, any local tissue
contractures and history of wrist trauma.
- Patients who will not consent to completing The visual analogue scale (VAS) for pain
or nerve conduction study before and after injection.