Pain outcome in patients undergoing RFA for varicose veins using different methods of anesthesia

A Randomised control trial to estimate the peri procedural pain outcome in patients undergoing Radiofrequency ablation for uncomplicated varicose veins under ultrasound guided femoral nerve block plus tumescent anesthesia in comparison to using only tumescent anesthesia in a tertiary care teaching centre in western India. - RFA

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/10/075347

Enrollment

Registered

2024-10-15

Start date

Unknown

Completion date

Unknown

Last updated

2024-11-11

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

Conditions

Health Condition 1: I839- Asymptomatic varicose veins of lower extremities Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Radiofrequency ablation of great sephanous vein in uncomplicated varicose veins: All the patients in this study will be undergoing RFA for uncomplicated varicose veins ,however, in one

Eligibility

Inclusion criteria

Inclusion criteria: Patients with uncomplicated varicose veins

Exclusion criteria

Exclusion criteria: complicated varicose veins,PAOD,DVT,recurrent cases, age less than 15 years

Design outcomes

Primary

Measure	Time frame
Peri-procedural pain outcome using vas scale ,period of restriction of limb movement and volume of aesthetic solution used in the procedure.Timepoint: Peri-procedural pain outcome at 5mins, 60mins, 6 hrs ,12hrs and 24hrs.	—

Secondary

Measure	Time frame
NilTimepoint: NIl	—

Countries

India

Contacts

Public ContactDr Jafar Husain

ARMED FORCES MEDICAL COLLEGE PUNE

jafarhusain01@gmail.com9632885396

Outcome results

None listed

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