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Melanotan-I

Afamelanotide, MT-I, [Nle4-D-Phe7]-α-MSH, Scenesse, CUV-1647

Quick Stats
Studies 225
Trials 100
Completed PHASE1, PHASE2 INTERVENTIONAL NCT01605383

Mesenchymal Stem Cells in Osteonecrosis of the Femoral Head

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

The present study evaluates the effect of XCEL-MT-OSTEO-ALPHA in osteonecrosis of the femoral head in comparison to the standard treatment of isolated core decompression. XCEL-MT-OSTEO-ALPHA is a tissue engineering product composed by "ex-vivo" expanded autologous mesenchymal stem cells fixed in allogenic bone tissue. The working hypothesis proposes that the tissue engineering is a valid and useful technique to achieve bone regeneration, avoiding the progression to collapse of the femoral head.

Detailed Description

Prospective, open-label with blinded assessor, randomized, parallel, single-dose phase I-II clinical trial in which 24 patients affected with osteonecrosis of the femoral head ARCO grade I or II will enter the trial with the primary objective of assessing the feasibility and safety of "ex-vivo" expanded autologous mesenchymal stem cells fixed in allogenic bone tissue in osteonecrosis of the femoral head. Secondary objectives are to assess the efficacy of the implantation by imaging (magnetic resonance imaging) and clinical questionnaires (pain by visual analogue scale, quality of life by SF-36 and WOMAC Index). Patients will be randomized to one of the two treatment arms (core decompression and the tissue engineering product composed by "ex-vivo" expanded autologous mesenchymal stem cells fixed in allogenic bone tissue or the standard treatment of isolated core decompression). Thereafter, patients will be followed for 12 months.

Interventions

Name: XCEL-MT-OSTEO-ALPHA
Type: BIOLOGICAL
Description: Core decompression plus XCEL-MT-OSTEO-ALPHA
Name: Standard treatment
Type: PROCEDURE
Description: Isolated core decompression

Primary Outcomes

Measure: Safety of XCEL-MT-OSTEO-ALPHA in osteonecrosis of the femoral head
TimeFrame: 12 months
Description: Safety will be assessed by collecting adverse events throughout the experimental phase, which includes a follow-up of 12 months
Measure: Feasibility of XCEL-MT-OSTEO-ALPHA in osteonecrosis of the femoral head
TimeFrame: 12 months
Description: Feasibility will be measured by assessing the percentage of patients to which bone marrow puncture is made are thereafter treated and by checking the cascade of procedures to confirm the global process is viable.

Trial Information

NCT ID

NCT01605383

Status

Completed

Study Type

INTERVENTIONAL

Phases

PHASE1, PHASE2

Sponsor

Banc de Sang i Teixits

Last Updated

December 15, 2025