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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01626755
Other study ID # PLATA
Secondary ID
Status Terminated
Phase N/A
First received June 21, 2012
Last updated October 25, 2017
Start date August 2013
Est. completion date April 2017

Study information

Verified date October 2017
Source Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Phantom limb pain following amputation is a major problem. Current evidence how to best prevent phantom limb pain is equivocal because previous trials have included small numbers of patients, and tested heterogeneous patient collectives. There is some evidence that optimized perioperative pain control is effective in preventing phantom limb pain, but the potential added role of regional anesthesia has not been defined.

Objective:

The Aim of this study is to test the hypothesis that sciatic nerve block decreases the point prevalence of phantom limb pain 12 months after transtibial amputation for peripheral vascular disease compared to optimized intravenous pain therapy.

Study design:

Randomized, prospective, double-blind (patient, physician, statistician) clinical trial. All patients will receive standard optimized intravenous anesthesia and analgesia (opiate patient-controlled analgesia (PCA), intravenous ketamine). Patients in the intervention group will receive additional infusion of local anesthetic via a sciatic nerve catheter placed under ultrasound guidance.

Main outcome of this study:

Point prevalence of chronic phantom limb pain after 12 months.


Description:

Rationale:

Phantom limb pain following amputation is a major clinical problem. Current evidence how to best prevent phantom limb pain is equivocal because previous trials have included small numbers of patients, and tested heterogeneous patient collectives. There is some evidence that optimized perioperative pain control is effective in preventing phantom limb pain, but the potential added role of regional anesthesia has not been defined.

Objective:

The Aim of this study is to test the hypothesis that sciatic nerve block decreases the point prevalence of phantom limb pain 12 months after transtibial amputation for peripheral vascular disease compared to optimized intravenous pain therapy.

Study design:

Randomized, prospective, double-blind (patient, physician, statistician) clinical trial. All patients will receive standard optimized intravenous anesthesia and analgesia (opiate patient-controlled analgesia (PCA), intravenous ketamine). Patients in the intervention group will receive additional infusion of local anesthetic via a sciatic nerve catheter placed under ultrasound guidance.

Study population:

Patients undergoing elective transtibial amputation for peripheral vascular disease at one of the participating centres, ASA status II to IV.

Intervention:

Infusion of local anesthetic via sciatic nerve catheter placed under ultrasound guidance.

Main study parameter/endpoint:

Point prevalence of chronic phantom limb pain after 12 months.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness:

All patients, regardless of group allocation, will receive optimalized intravenous pain treatment. The aim of this study is to assess whether additional regional anesthesia (ultrasound-guided sciatic nerve block) can decrease the incidence of phantom limb pain. The working hypothesis is that patients undergoing intervention treatment (optimized intravenous therapy plus nerve block) are expected to feature a decreased incidence of phantom limb pain at 12 months, in addition to improved perioperative analgesia.

The administration of both optimalized intravenous pain treatment and peripheral nerve blockade is routine clinical practice for many procedures on the lower leg, including amputation. The risk of this intervention can be described as very low. In control patients, the sciatic catheter will be used for rescue pain treatment.


Recruitment information / eligibility

Status Terminated
Enrollment 12
Est. completion date April 2017
Est. primary completion date April 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients undergoing elective transtibial amputation for peripheral vascular disease

- age over 18 years

- American Society of Anaesthesiology status II to IV

Exclusion Criteria:

- contraindication to peripheral regional anesthesia

- psychiatric disease

- pregnancy or breastfeeding status

- amputation for tumour surgery

- traumatic amputation

- inability to give written and informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Sciatic name block
Ultrasound-guided sciatic nerve block.

Locations

Country Name City State
Austria Innsbruck Medical University Hospital Innsbruck Tirol
Austria General Hospital Klagenfurt Klagenfurt Carinthia
Belgium Ziekenhuis Oost Limburg Genk Limburg
Netherlands Academic Medical Center, University of Amsterdam Amsterdam Noord-Holland
Netherlands Westfriesgasthuis Hoorn Noord-Holland
Netherlands Canisius Wilhelmus Ziekenhuis Nijmegen
Netherlands Erasmus Medical Center Rotterdam Noord-Holland
Spain Valencia University Hospital Valencia
United States Massachusetts General Hospital, Dept. of Anesthesiology, Perioperative and Pain Medicine Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) European Society of Anaesthesiology

Countries where clinical trial is conducted

United States,  Austria,  Belgium,  Netherlands,  Spain, 

References & Publications (2)

Rathmell JP, Kehlet H. Do we have the tools to prevent phantom limb pain? Anesthesiology. 2011 May;114(5):1021-4. doi: 10.1097/ALN.0b013e31820fc80d. — View Citation

Ypsilantis E, Tang TY. Pre-emptive analgesia for chronic limb pain after amputation for peripheral vascular disease: a systematic review. Ann Vasc Surg. 2010 Nov;24(8):1139-46. doi: 10.1016/j.avsg.2010.03.026. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Point prevalence of chronic phantom limb pain 12 months after amputation
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