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A study to find the role of lignocaine given in intravenous route to manage the pain of fibromyalgia patients.

Effect of desensitisation with intravenous lignocaine in fibromyalgia patient - a prospective study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/08/020614
Enrollment
50
Registered
2019-08-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M797- Fibromyalgia

Interventions

Intervention1: Desensitisation with intravenous lignocaine: 5 mg/kg body weight Lignocaine (2%) preservative free will be given intravenously with 100 ml normal saline over 1 hour. It will be given fo

Sponsors

ESI Institute of Pain Management
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients suffering from fibromyalgia with Widespread Pain Index(WPI)more than 7 and Symptom Severity Index(SSS) more than 5 or WPI 4-6 and SSS more than 9 2. Duration of fibromyalgia more than 12 weeks 3. Patient taking anti-neuropathic medicine more than 4 weeks 4. Degree of pain more than 5 according to VAS

Exclusion criteria

Exclusion criteria: 1. Patients with allergy to lignocaine 2. History of cardiac dysrrythmias 3. Patients with severe hepatic and renal disease 4. Patients not giving consent 5. Poorly controlled psychiatric conditions with possible secondary gain or severe comorbidity.

Design outcomes

Primary

MeasureTime frame
Widespread Pain Index(WPI) and Symptom Severity Index(SSS)Timepoint: will be noted prior to the procedure and 1, 4 and 6 weeks after the procedure.

Secondary

MeasureTime frame
Brief Pain Inventory(BPI) scoreTimepoint: will be noted prior to the procedure and 1, 4 and 6 weeks after the procedure.;Pain score using Visual Analogue ScaleTimepoint: will be noted prior to the procedure and 1, 4 and 6 weeks after the procedure.

Countries

India

Contacts

Public ContactDr Subrata Goswami

ESI Institute of Pain Management

drsgoswami@gmail.com09830430430

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026