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A higher response of plasma neuropeptide Y, growth hormone, leptin levels and extracellular glycerol levels in subcutaneous abdominal adipose tissue to Acipimox during exercise in patients with bulimia nervosa: microdialysis study

Antilipolytic drug Acipimox during short-term exercise further increases plasma neuropeptide Y levels in patients with bulimia nervosa compared with healthy women: the role of lipolysis

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000955910
Enrollment
16
Registered
2011-09-06
Start date
2008-01-08
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Interventions

All subjects were randomised to receive either placebo or Acipimox capsules each week (two 250 mg capsules of the acute-bolus Aci therapy or placebo; 500 mg total - 5- Methylpyrazine-2-carboxylic acid 4-oxide, Olbetam capsules, Farmitalia Carlo Erba, Italy) 500 mg orally 1 hour before a single exercise bout, once a week over a total of 2 weeks. A low- to moderate-intensity exercise bout on an electromagnetically braked bicycle ergometer (Cateye EC 1600, Japan) was performed for 45 min at power o

All subjects were randomised to receive either placebo or Acipimox capsules each week (two 250 mg capsules of the acute-bolus Aci therapy or placebo; 500 mg total - 5- Methylpyrazine-2-carboxylic acid 4-oxide, Olbetam capsules, Farmitalia Carlo Erba, Italy) 500 mg orally 1 hour before a single exercise bout, once a week over a total of 2 weeks. A low- to moderate-intensity exercise bout on an electromagnetically braked bicycle ergometer (Cateye EC 1600, Japan) was performed for 45 min at power output 2 W/kg of lean body mass (LBM). All subjects during 45-min exercise were connected personally with their nurses and attending physicians.

Sponsors

Ministry of Health
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

age between 18 and 30 years, BMI between 18 and 23 kg/m2, patients with a diagnosis of bulimia nervosa (Diagnostic and Statistical Manual of Mental Disorders, DSM-IV, 1994)

Exclusion criteria

hypertension, abnormal blood tests with significant hyperlipidaemia, history or presence of hepatic or renal disorders All eligible participants were deemed healthy.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 27, 2026