Alprostadil
Drug- Active Substance: Prostaglandin E1
- Pharmaceutical Form: solution for infusion
- Concentration: 40 μg b.d.
- Route of Administration: intravenous infusion
Other names: Prostavasin
NCT Number: NCT00596752
The study is to confirmatorily show a superior effect of Alprostadil compared to placebo on the rate of complete healing of ischemic necroses and ulcerations as well as on the frequency and height of major amputations in patients suffering from PAOD stage IV.
Looking for future studies?
Notify Me45 year and older
All sexes
Interventional
Phase 4
404, Pilsen, Czechia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: Prostavasin
Time frame: At 12 weeks after the end of study drug treatment
The assessment of ulcer area was collected per lesion with up to 2 lesions per subject (both legs could be affected). In the analysis a subject is only considered completely healed at a time point, if all ischemic lesions are reported as completely healed at that time point.
Time frame: At 24 weeks after the end of study drug treatment
Assessment of amputations was collected per leg affected by a lesion with up to 2 lesions per subject. Amputations were regarded as major if they were performed at the ankle joint level or above. Amputations of toes or part of the foot leaving a stump thereon the subject can walk were regarded as minor. An affected leg is defined as a leg with at least 1 lesion on Study Day -6 to -2 and only amputations of affected legs are considered in the efficacy analysis of amputations. A subject is counted as major/minor amputated, if at least 1 affected leg was major/minor amputated.
Time frame: At 24 weeks after the end of study drug treatment
The assessment of ulcer area was collected per lesion with up to 2 lesions per subject (both legs could be affected). In the analysis a subject is only considered completely healed at a time point, if all ischemic lesions are reported as completely healed at that time point.
Time frame: At 24 weeks after the end of study drug treatment
Visit values of intensity of rest pain from a visual analogue scale, ranging from 0 mm (no pain) to 100 mm (maximum conceivable pain), had to be reported in the case of presence of rest pain only. If the leading question in regard to the presence of rest pain is answered with "No" and no visit value is specified, the visit value will be set to 0 for the analysis.
Time frame: At 24 weeks after the end of study drug treatment
In case of two ulcers the worse ulcer status is analyzed. The categories of investigator assessment are: complete healing, decrease by ≥ 50 %, unchanged, increase by ≥ 50 %.
Time frame: During the course of the study (up to 196 days)
The number of subjects who used analgesics are summarized for different time points/intervals during the course of the study.
Time frame: At 24 weeks after the end of study drug treatment
Systolic pressure at ankle level was measured at the Arteria tibialis posterior and the Arteria dorsalis pedis. Two individual series of measurements of arterial pressures per subject across the assessed visits were selected for the analysis. For the first analysis (worst change analysis) the series of measurements in the one artery which has the worst change from Baseline at the final measurement was used. For the second analysis (worst value analysis) the series of measurements which has the worst final post-Baseline measurement was used. The series relevant for the analyses was selected from the series for the affected leg or legs only. The selection is 1 out of up to 4 series available per subject. Series without Baseline value and series with at least 1 measurement of more than 150 mmHg were excluded from the selection process due to the suspicion of media sclerosis of the lower limb artery.
Time frame: At 24 weeks after the end of study drug treatment
Assessment of amputations was collected per leg affected by a lesion with up to 2 lesions per subject. Amputations were regarded as major if they were performed at the ankle joint level or above. Amputations of toes or part of the foot leaving a stump thereon the subject can walk were regarded as minor. An affected leg is defined as a leg with at least 1 lesion on Study Day -6 to -2 and only amputations of affected legs are considered in the efficacy analysis of amputations. A subject is counted as major/minor amputated, if at least 1 affected leg was major/minor amputated.
The number of subjects with minor amputation prior to or at 24 weeks after the end of study drug treatment is presented below.
Time frame: At 24 weeks after the end of study drug treatment
The number of subjects with revascularization prior to or at 24 weeks after the end of study drug treatment is presented below.
Time frame: During the course of the study (up to 196 days)
Time frame: During the course of the study (up to 196 days)
Time frame: During the course of the study (up to 196 days)
Cardiovascular morbidity is presented as number of subjects with myocardial infarction and/or stroke during the course of the study.
UCB BIOSCIENCES GmbH
Industry
Multinational, Prospective, Randomized, Double-Blind, Placebo-Controlled, Parallel Groups Study to Assess the Efficacy and Safety of Prostaglandin E1 in Subjects With Critical Limb Ischemia (Fontaine Stage IV)
Acronym: ESPECIAL
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02460042
Peripheral Arterial Occlusive Disease, Peripheral Arterial Occlusive Disease 1
Berlin, Germany
View Trial DetailsNCT07093632
Arterial Bypass Surgery, Arterial Occlusive Diseases
Lyon, France
View Trial DetailsNCT02189018
Arterial Occlusive Diseases, Arteriosclerosis
Baltimore, Maryland, United States
View Trial DetailsNCT01855412
Peripheral Arterial Occlusive Disease, Peripheral Arterial Occlusive Disease 1
Gilbert, Arizona, United States
View Trial Details