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GrUVen-I Study

Human Recombinant Epidermal Growth Factor in patients with venous ulcers.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
RPCEC
Registry ID
RPCEC00000106
Enrollment
50
Registered
2011-05-03
Start date
2005-12-04
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Venous ulcers.

Interventions

The test product was administered topically to the lesion, 3 times a week (after the treatment with physiological saline) for 8 to 12 weeks, according to the randomization of patients. Group I: viscou

Sponsors

Center for Genetic Engineering and Biotechnology (CIGB), in Havana.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Informed consent of patient. 2.Age major than 18 years old. 3.Diagnosis of an only venous ulcer in lower limbs, not infected, up to 1 cm2 and minor than 10 cm2.

Exclusion criteria

Exclusion criteria: 1.Diabetes mellitus, Sickle Cell anemia. 2.Cancer (except the basal cell carcinoma and the cervix cancer in situ after surgery and complete cured). 3.Metabolic disease (liver disease, renal disease, pancreatic diseases, colagenosis) Mild o serious anemia (Hb = 11 g/L for women y 12 g/L for men). 4.Severely disabled (caquexia, critical patients, life-threatening diseases). 5.Uncontrolled Hypertension due to clinical examination. 6.Peripheral arterial chronic diseases referred by patient and confirm bay clinical examination. 7.Patients treated with steroids in the last 3 months. 8.Patients treated with EGF in the last 30 days. 9.Serious psychiatric disorder and other disease that limit informed consent. 10.Pregnancy or nursery.

Design outcomes

Primary

MeasureTime frame
Clinical response (taking into account the percentage of healing): Total Response: more than 90% of healing. Parcial Response: between 50% and 90% of healing. Minimal Response: between 25% and 50% of healing. Not response: less than 25% of healing. Progression: increment in size or deep, or complications. Measurement time, weekly (first 8 weeks) and at week 12.

Secondary

MeasureTime frame
Healing time in days after injury at the end of treatment. Epithelialized area, weekly until treatment ends. Daily recovery rate of the affected area at the end of treatment. Presence of granulation tissue at the end of treatment. Quality of healing at the end of treatment and follow-up year.

Countries

Cuba

Contacts

Public ContactPedro López Saura

Center for Genetic Engineering and Biothecnology (CIGB).

lopez.saura@cigb.edu.cu

Outcome results

None listed

Source: RPCEC (via WHO ICTRP) · Data processed: Sep 19, 2026