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Study identifier: NCT05947136 Synced from ClinicalTrials.gov · July 28, 2026
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PASCA-MM Study. Impact of the PASCA (PArcours de Santé au Cours du CAncer) Program on Complications Associated With Multiple Myeloma and/or Its Treatments in the Context of a First Hematopoietic Stem Cell Autograft, in Adults Aged 18 to 70.

Condition: Multiple Myeloma · Complication  ·  Sponsor: Centre Leon Berard

PhaseNA
Planned participants204
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

This is a prospective, multicentre, phase III, randomised, controlled intervention study. Two groups of patients with equal numbers will be studied and each patient will be allocated to one of the two groups described below by randomisation (ratio 1:1). Each patient will be allocated to one of the two groups described below by randomisation (ratio 1:1). \- PASCA interventional group For both the 7 complications of interest (primary objective) and the 13 secondary complications (secondary objective), a specific and proactive referral will be made systematically after each screening assessment, depending on the level of risk, estimated according to decision trees (management guide) and through the dedicated PASCA network of healthcare professionals, in order to initiate early treatment and follow-up if necessary. \- Control group For the 7 complications of interest (primary objective) as well as for the 13 complications (secondary objective): all the data from each identification check-up will be sent to the onco-haematological transmitted to the referring onco-haematologists, so that they can initiate their own management. =\> For all patients, regardless of group All patients will receive four screening assessments covering the 7 complications of interest and 13 secondary complications: * Visit No.1 (T1), 1-2 months after the autologous haematopoietic stem cell transplantation (aHSCT), corresponding to the patient's visit to his or her Multiple Myeloma (MM) monitorin…

This description comes directly from the study's public registry record.

Talk to the study team

Romain BUONO, PharmaD, MPH  ·  +33469856358  ·  romain.buono@lyon.unicancer.fr

Meyssane DJEBALI, Msc  ·  ++33426556743  ·  meyssane.djebali@lyon.unicancer.fr

Always discuss trial participation with your own doctor first.

Locations (6)

CH Annecy GenevoisÉpagny, FranceRecruiting
CHU La TroncheGrenoble, FranceRecruiting
Centre Léon BérardLyon, FranceRecruiting
CENTRE HOSPITALIER UNIVERSITAIRE de MONTPELLIERMontpellier, FranceRecruiting
CHU de St-EtienneSaint-Etienne, FranceRecruiting
Le Centre Hôpitaux Nord-Ouest Villefranche-sur-SaôneVillefranche-sur-Saône, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT05947136