CClinicalTrials.gg
Status unknownNCT01022177Updated Dec 2, 2011

Influence of Acupuncture to Ocular Microcirculation in Patients With Diabetes Mellitus

A Phase 2 interventional study of acupuncture in Diabetes Mellitus, Type 2, sponsored by Technische Universität Dresden. Status unknown at 1 site in Germany. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-12-02.

Sponsored by Technische Universität Dresden · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2011), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
40
Allocation
Non-randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

The purpose of this study is to determine the influence of specific eye acupuncture to the ocular microcirculation in diabetic and healthy subjects.

Read the detailed description

Diabetes is combined with severe vascular damage at the different stages of the disease, causing reduction in retinal perfusion. Acupuncture is supposed to regulate the perfusion. We propose a study to evaluate the effect of acupuncture to the vascular auto regulation in patient with Diabetes, compared to healthy people without vascular or retinal diseases. The perfusion of the retinal vessel will be examined by Retinal vessel analyzer (RVA), Heidelberg retinal Flowmeter (HRF) and the Ocular blood Flowmeter (OBF) before, during and after standardized specific acupuncture at healthy volunteers and patients with diabetes.

02

Conditions studied

  • Diabetes Mellitus, Type 2
03

In context

Diabetes Mellitus

10,923 studies on the registry are indexed under Diabetes Mellitus; 1,318 are open to participants now.

This study's planned enrollment of 40 is below the median of 80 across 8,367 interventional studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

Technische Universität Dresden is the lead sponsor of 237 studies on the registry; 45 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • persons over 18 years, men or women, diabetic diagnostics within the last year

Exclusion criteria

Exclusion Criteria:

  • medical use of anticoagulative substances, use of dorzolamide, use of immunosuppressive medication
  • psychiatrics, epileptics
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Active comparator
    diabetics

    subjects with HbA1c \>7,0 and pathological glucose tolerance testing

    Procedure: acupuncture

  • Active comparator
    healthy

    healthy subjects with HbA1c \<7,0 and negative glucose tolerance testing

    Procedure: acupuncture

Interventions

  • Procedureacupuncture

    acupuncture of the eye in traditional chinese schematics

    Also known as: acupuncture therapy

06

What researchers measure

Primary outcomes

  1. retinal perfusion by HRF/OBF/RVA

    Time frame: post acupuncture (one day measurement)

07

Study locations

1 of 1 sites recruiting
  • University Carl Gustav Carus
    Dresden, Saxonia 01307, Germany
    • Kathleen - Wozniak, - · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 2, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01022177
Lead sponsor
Technische Universität Dresden
First posted
Dec 1, 2009
Start date
Oct 2009
Primary completion
Oct 2010
Completion
May 2012 (estimated)
Last update
Dec 2, 2011

Study contacts

Janek - Haentzschel, Dr.
Contact
Janek.Haentzschel@uniklinikum-dresden.de
0351-4583381
Kathleen - Wozniak, -
Contact
Kathleen.Wozniak@uniklinikum-dresden.de
0351-4583381
Janek - Haentzschel, Dr.
study director

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2011. You cannot join it, but the record below documents what was studied.

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