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Intermittent ClaudicationPhase 2NCT01256775

Effect of NCX4016 on Walking Distance in Patients With Peripheral Arterial Occlusive Disease (PAOD)

A Phase 2 study testing NCX-4016 in people with Intermittent Claudication, run by NicOx Research Institute S.r.l. at 1 site in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Peripheral arterial disease (PAD) is almost invariably associated with a generalized atherosclerotic involvement of the arterial tree and endothelial dysfunction. Previous short term studies showed improvement of vascular reactivity and walking capacity in PAD patients by measures aimed at restoring Nitric Oxide (NO)… Read more about this study

Who is it for?
Ages 40 to 80 years
Conditions the study is for
Intermittent Claudication
What is being tested?
NCX-4016
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
442 participants
Where
1 siteItaly
Study dates
Sep 2003to Apr 2005
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • male and female patients between 40 and 80 years with Leriche-Fontaine stage II PAD presenting symptoms of intermittent claudication stable for at least 6 months
  • ankle/brachial index <0.9
  • an absolute claudication distance (ACD) <500 m
  • an initial claudication distance (ICD) >50 m on a standardized treadmill test (3% incline, 3 km/hr)
  • and clinical stability before inclusion (i.e. changes in ACD not exceeding 25% in two standardized treadmill tests during run-in).
  • all patients gave their written informed consent.

Who cannot join

  • unstable symptoms and/or rapid deterioration of PAD during the previous 3 months
  • presence of clinically significant renal or hepatic failure, or insulin-dependent type 1 diabetes
  • uncontrolled type 2 diabetes, arterial hypertension or dyslipidemia
  • any clinical condition limiting the patient's exercise ability (angina pectoris, congestive heart failure, respiratory disease, bone and joint disease, neurological disorders)
  • active peptic ulcer during the previous 6 months
  • any hemorrhagic condition or history of bleeding
Show all 15Show fewer
  • acute coronary syndrome or acute cerebrovascular episodes during the previous 6 months
  • previous revascularization procedures during the last 6 months or indication for vascular surgery; ischemic rest pain
  • life expectancy <12 months
  • pregnancy or lactation
  • participation to other investigational trials within 3 months prior to inclusion
  • history of hypersensitivity or any form of allergic reaction or contraindications to NSAIDs, aspirin, and NO-donating drugs
  • the following treatments were not allowed for the period of the study: continuative use (>7 days) of NSAIDs or nitrovasodilating drugs
  • phosphodiesterase type 5 inhibitors, anticoagulants, heparin, ticlopidine, clopidogrel, indobufen, defibrotide, mesoglycan, picotamide, pentoxyfylline, carnitine, sulodexide
  • All other concomitant treatments were kept constant as much as possible during the study period.

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • Ospedale di Perugia

    Perugia, Italy, 06126

Other trials in Italy

About this study

Official title: A Multicenter, Double-blind, Randomized, Parallel Group Study to Assess the Effect of NCX4016 vs Placebo on Walking Distance in Patients With Peripheral Arterial Occlusive Disease at Leriche-Fontaine Stage II

Peripheral arterial disease (PAD) is almost invariably associated with a generalized atherosclerotic involvement of the arterial tree and endothelial dysfunction. Previous short term studies showed improvement of vascular reactivity and walking capacity in PAD patients by measures aimed at restoring Nitric Oxide (NO) production. NO is also known to prevent the progression of atherosclerosis. We wished to assess whether the prolonged administration of a NO-donating agent (NCX 4016) improves the functional capacity of PAD patients and affects the progression of atherosclerosis as assessed by carotid intima-media thickness (IMT).

Four hundred forty two patients with stable intermittent claudication were enrolled in a prospective, double blind, placebo-controlled study and randomized to either NCX 4016 800mg bid or its placebo for 6 months. The primary study outcome was the absolute claudication distance (ACD) on a constant treadmill test (10% incline, 3km/hr); main secondary end-point was the change of the mean far-wall right common carotid artery IMT.

Read the detailed description

Design of the study This was a prospective, randomized, double-blind, parallel-groups, placebo-controlled study conducted in fortythree clinical sites throughout Europe. 442 patients with peripheral arterial occlusive disease (PAD) at Leriche-Fontaine stage II were treated with NCX 4016 800 mg bid or with an indistinguishable placebo for 6 months. The dosage of 800 mg bid was selected based on previous clinical studies, which demonstrated a good safety profile and a good tolerability in the gastro intestinal tract. Compliance was checked by counting dispensed versus returned study medication.

All patients received 100 mg aspirin once daily for cardiovascular prevention, standard for this patient population at the time of study design.

Inclusion criteria were: male and female patients between 40 and 80 years with Leriche-Fontaine stage II PAD presenting symptoms of intermittent claudication stable for at least 6 months, an ankle/brachial index <0.9, an absolute claudication distance (ACD) <500 m and an initial claudication distance (ICD) >50 m on a standardized treadmill test (3% incline, 3 km/hr), and clinical stability before inclusion (i.e. changes in ACD not exceeding 25% in two standardized treadmill tests during run-in). All patients gave their written informed consent.

Exclusion criteria were: unstable symptoms and/or rapid deterioration of PAD during the previous 3 months; presence of clinically significant renal or hepatic failure, or insulin-dependent type 1 diabetes; uncontrolled type 2 diabetes, arterial hypertension or dyslipidemia; any clinical condition limiting the patient's exercise ability (angina pectoris, congestive heart failure, respiratory disease, bone and joint disease, neurological disorders); active peptic ulcer during the previous 6 months; any hemorrhagic condition or history of bleeding; acute coronary syndrome or acute cerebrovascular episodes during the previous 6 months; previous revascularization procedures during the last 6 months or indication for vascular surgery; ischemic rest pain; life expectancy <12 months; pregnancy or lactation; participation to other investigational trials within 3 months prior to inclusion; history of hypersensitivity or any form of allergic reaction or contraindications to NSAIDs, aspirin, and NO-donating drugs. The following treatments were not allowed for the period of the study: continuative use (>7 days) of NSAIDs or nitrovasodilating drugs; phosphodiesterase type 5 inhibitors, anticoagulants, heparin, ticlopidine, clopidogrel, indobufen, defibrotide, mesoglycan, picotamide, pentoxyfylline, carnitine, sulodexide. All other concomitant treatments were kept constant as much as possible during the study period.

Primary end-point of the study was the ACD on a constant treadmill test; secondary end-points were ICD; responder rates, i.e. the proportion of patients showing a >=28% or a >=50% improvement of ACD in comparison with baseline; quality of life questionnaire Short-Form 36 (SF-36); the variations of the ankle/brachial index (ABI) between baseline and 6 months and the modifications of the intimal medial thickness (IMT) of the common right carotid artery at 6 months as compared with baseline.

Common right carotid artery was examined by B-mode ultrasound in the longitudinal view, 1-1.5 cm proximally to the bifurcation. The measurement of IMT was obtained according to the Mannheim carotid intima-media thickness consensus with one modification: instead of acquiring the vascular wall image only with the lateral probe incidence, images were acquired also with the anterior and posterior incidence, in order to obtain a triplicate number of measurements to be used for comparisons. Each position was visualized and recorded for at least 15 sec. with simultaneous taking of the ECG tracing. Images of the far wall of the distal 1 cm of the right common carotid artery were obtained. IMT was calculated from each of the three projections and the final value was calculated from the average of all measurements with the use of standardized ultrasonography settings. The baseline carotid ultrasonographic examinations were used to localize the site of interest at follow-up. Digitized still images from an electrocardiographically defined diastolic frame were analyzed offline. A single observer who was unaware of the treatment assignments and the identities of the patients measured the mean carotid intima media thickness. Focal atherosclerotic plaques were excluded from the measurements. All measurements were performed with the use of an automated border detection system. A number of measurements not inferior to 30 for each of the three image acquisition incidences was carried out in the 1cm segment of the carotid artery assessed. For each subject the same ultrasound system and transducer and the same operator were used throughout the study. Images were centrally analyzed at the coordinating center by a dedicated, automated computerized edge detection system for the measurement of common carotid far wall intima-media using the software M'ATH 2.0 (Metris Argenteuil, France).

Being tested
NCX-4016, NCX4016 placebo
Keywords
atherosclerosis, carotid intima-media thickness, intermittent claudication, Nitric Oxide / NO
Medical subject headings
Intermittent Claudication, Atherosclerosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • NCX-4016Drug

    NCX4016 800 mg b.i.d. for 6 months on top of aspirin 100 mg o.d.

  • NCX4016 placeboDrug

    NCX4016 placebo b.i.d. for 6 months

Study groups in NCT01256775
Study groupRoleWhat they receive
NCX4016 placeboPlacebo comparatorNCX4016 placebo b.i.d for 6 months
Receives: Drug: NCX4016 placebo
NCX4016Active comparatorncx4016,800 mg b.i.d., on top of aspirin 100 mg o.d.
Receives: Drug: NCX-4016

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. maximal walking distance evaluated by a constant treadmill test

    Measured: baseline

  2. maximal walking distance evaluated by a constant treadmill test

    Measured: 6 months

Secondary outcomes (2)
  1. pain-free walking distance

    Measured: baseline, 1-3-6 months

  2. assessment of carotid artery IMT

    Measured: baseline and 6 month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Dec 2010 (estimated)
  2. Study startSep 2003
  3. Primary completionApr 2005
  4. Study completionApr 2005

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
442 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01256775
Sponsor's protocol ID
NCX4016-X-208
Status last verified
Jan 2011
First submitted
6 Dec 2010
Last updated
19 Jan 2011
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing NCX-4016 in people with Intermittent Claudication, run by NicOx Research Institute S.r.l. at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 15 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Jan 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

maximal walking distance evaluated by a constant treadmill test (time frame: baseline). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Jan 2011.

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