Single-port thoracoscopic sympathicotomy for treatment of complex regional pain syndrome type I, a feasibility study.

Single-port thoracoscopic sympathicotomy for treatment of complex regional pain syndrome type I, a feasibility study. - SPTS in CRPS

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON36901

Enrollment

Registered

2012-11-28

Start date

2012-12-01

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

posttraumatic dystrophy posttraumatic paindydrome

Interventions

Unilateral single-port VATS sympathicotomy on T2-T5 level.

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: CRPS-I refractory to standard treatment Age 18-65 years

Exclusion criteria

Exclusion criteria: COPD > Gold I >20 packyears smoking Previous thoracic surgery on affected side

Design outcomes

Primary

Measure	Time frame
Pain, measured in Visual Analoque Scale (VAS)-Score	—

Secondary

Measure	Time frame
- Function in the extremity (RASQ-questionnaire and function tests) - Health Related Quality of Life (SF-36 questionnaire)	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)