Randomized Study of Pregabalin for Pain Reduction in Patients With Rest Pain and Lower Limb Ischemia

Karolinska Institute

Status and phase

Terminated

Phase 4

Conditions

Critical Limb Ischemia

Ischemia

Arterial Occlusive Disease

Pain

Treatments

Drug: pregabalin

Drug: placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT00403780

PREPARED_00

Details and patient eligibility

About

The hypothesis behind the trial is the concept that Pregabalin is effective in reducing pain at rest in lower limb ischemia, and the study evaluates active treatment or placebo added to the regular pain regimens for these patients.

Full description

Critical limb ischemia (CLI) is the end stage of peripheral arterial disease in the legs and is a consequence of deteriorating blood flow supply to the lower limbs. The clinical definition of CLI includes peripheral arterial disease and recurrent rest pain for at least two weeks with or without ulcers or gangrene.

In patients not amenable to revascularization - around 35% - amputation or palliative conservative care remains the options. Pain control is a vital part of any treatment of these patients. Besides being the principal conservative treatment, also patients undergoing revascularization experience severe pain both during work up and after surgery.

Experimental data indicate that pain in CLI is multimodal and to a large extent neuropathic. Still, current therapy is mostly based on opioid treatment, which clinically often affects pain moderately. The doses required to influence pain are also associated to severe side effects. Accordingly, there is a great need to improve pain control in the rather common disease CLI.

comparisons: pregabalin up to 600mg daily in addition to regular pain regimens compared to placebo and regular pain regimens.

Enrollment

18 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

Rest pain, gangrene or ulcers located below the patella for a duration of at least two weeks (either one of these criteria are sufficient).
One measurement of: Ankle blood pressure(ABP) <70 mm Hg, an toe blood pressure(TBP) <50, or a TcPO2<45 mm Hg, or an ankle/brachial pressure index <0.7 (either one of these criteria are sufficient).
Informed consent obtained

Exclusion criteria

Age < 55 years
Women of childbearing potential
Patients already medicating with Pregabalin or Gabapentin
Creatinine clearance <30ml/min
Amputation necessary within two weeks
Revascularization necessary within two weeks (open vascular surgery or endovascular)
A medical history of clear dizziness
NYHA class IV heart failure
Known hypotension, or having a systolic arm blood pressure <120 mm Hg (two consecutive measurements with the patient lying supine)
Simultaneous or previous (within 30 days prior to study entry participation in a clinical study using experimental drugs or devices
Mental condition making the subject unable to understand the concepts and risk of the study
Known allergies against pregabalin