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the Effectiveness of Intermittent Pneumatic Compression on Neuropathic Pain in Patients With Diabetic Polyneuropathy

B

Busra Gunes

Status

Completed

Conditions

Diabetic Neuropathic Pain

Treatments

Other: pregabalin group
Device: intermittent pneumatic compression +pregabalin group

Study type

Interventional

Funder types

Other

Identifiers

NCT06336486
BalikesirU-FTR-BG-01

Details and patient eligibility

About

In this study,the effectiveness of intermittent pneumatic compression therapy on neuropathic pain and quality of life in patients with neuropathic pain due to type 2 diabetes was investigated

Full description

The investigators conducted our research from 50 patients with type 2 diabetes of 5-20 years, who received pregabalin treatment with diabetic neuropathy with consent form between 40-75 years.The investigators divided the patients into two equal groups , some of the patients were given an intermittent pneumatic compression program at a pressure of 35 mmhg for 30 min to the lower extremity for 10 days of extreme alternation in our clinic and pregabalin treatment was continued,only pregabalin treatment of the other group was continued. VAS, PQAS, LANSS, SF-36 were evaluated.The evaluation was done before the treatment, at the end of the intermittent pneumatic compression treatment(approximately 2 weeks after the start of the treatment) and 3 months later.

Enrollment

50 patients

Sex

All

Ages

40 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 5-20 years history of type 2 diabetes
  • Between the ages of 40-75
  • Body mass 25-40
  • Blood pressure 100/60-140/90
  • Patient diagnosed with diabetic polyneuropathy
  • Use of pregabalin

Exclusion criteria

  • Connective tissue disease
  • Peripheral nerve vasculitis
  • Postherpetic neuralgia
  • Alcoholic neuropathy
  • Autonomic neuropathy
  • Chronic renal failure
  • Charcot-marie tooth disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

intermittent pneumatic compression +pregabalin
Active Comparator group
Description:
Patients were given an intermittent pneumatic compression program at a pressure of 35 mmhg for 30 min to the lower extremity for 10 days of extreme alternation in our clinic and pregabalin treatment was continued.
Treatment:
Device: intermittent pneumatic compression +pregabalin group
pregabalin
Other group
Description:
only pregabalin treatment was continued.
Treatment:
Other: pregabalin group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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