Application of Medical Imaging Procedures in Surgery Implanting in Cancerology With the Aim to Reduce Invasive Acts (ATIM)
21. juni 2011 opdateret af: Centre Leon Berard
Aero digestive Cancer patients treated by external head and neck radiotherapy and/or by curie-therapy and/or mandible reconstruction by microanastomosed fibula flaps.
The purpose of the study is to Investigate the accuracy of implants insertion in the anteroposterior way, using radiosurgical guidance.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
- Investigate the accuracy of inserting implants in the vertical way and in angulation, on irradiated native mandible or on microanastomosed fibula flaps
- Investigate the accuracy of inserting implants in the anteroposterior way, in the vertical way and in angulation for all the involved patients (meaning on irradiated native mandible or on microanastomosed fibula flaps)
- Investigate the delay of mucous healing
- Estimate the prosthetic function
- Evaluate the osteonecrosis rate after radiation with traumatic etiology due to implantation
- Estimate the implant rate due to minimally invasive flaps
- Estimate the implant rate due to pure trans mucosa way
- Estimate the post surgical therapeutic success after 1 year
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
53
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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-
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Clermont-ferrand, Frankrig, 63 000
- CHU Hôtel-Dieu Service d'Odontologie
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Lyon, Frankrig, 69007
- Hospices Civils de Lyon Service de Consultations et Traitements Dentaires
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Pierre Benite, Frankrig, 69495
- Centre Hospitalier Lyon Sud Service de Stomatologie et Chirurgie Maxillo-Faciale
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Cedex 08
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Lyon, Cedex 08, Frankrig, 69373
- Centre Léon Bérard Service de Chirurgie-Stomatologie
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- age over 18
- Performance status over 70
- Histological evidence of upper digestive tract cancer
- History of cranial / facial radiotherapy or brachytherapy and/or microvascular fibula transfer.
- Bone volume sufficient to support an implant.
- Mandatory affiliation with a social security system
- Written, voluntary, informed consent
Exclusion Criteria:
- Patient with evolutive malignant disease
- Contraindication to general anesthesia
- Concurrent disease contra-indicating implant surgery (risk of infectious endocarditis, uncontrolled diabetes, HIV, evolutive neoplasia…)
- Patient enrolled in another clinical trial including chemotherapy
- Pregnant or lactating woman
- Anticipation of an impossible follow-up
- Patient deprived of freedom
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Accuracy of implants insertion, radio-surgical guidance.
Tidsramme: 8 months after inclusion
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8 months after inclusion
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Accuracy of inserting implants
Tidsramme: 16 months after inclusion
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16 months after inclusion
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Delay of mucous healing
Tidsramme: 16 months after inclusion
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16 months after inclusion
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Estimation of the prosthetic function
Tidsramme: 16 months after inclusion
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16 months after inclusion
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Osteonecrosis rate after radiation with traumatic etiology due to implantation
Tidsramme: 16 months after inclusion
|
16 months after inclusion
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Implant rate
Tidsramme: 16 months after inclusion
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16 months after inclusion
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Post surgical therapeutic success after 1 year
Tidsramme: after 1 year
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after 1 year
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Anne-Gaëlle BODARD, MD, Centre Leon Berard
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
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- Marunick MT, Leveque F. Osteoradionecrosis related to mastication and parafunction. Oral Surg Oral Med Oral Pathol. 1989 Nov;68(5):582-5. doi: 10.1016/0030-4220(89)90244-2.
- Medin PM, Solberg TD, De Salles AA, Cagnon CH, Selch MT, Johnson JP, Smathers JB, Cosman ER. Investigations of a minimally invasive method for treatment of spinal malignancies with LINAC stereotactic radiation therapy: accuracy and animal studies. Int J Radiat Oncol Biol Phys. 2002 Mar 15;52(4):1111-22. doi: 10.1016/s0360-3016(01)02762-6.
- Parel SM, Triplett RG. Interactive imaging for implant planning, placement, and prosthesis construction. J Oral Maxillofac Surg. 2004 Sep;62(9 Suppl 2):41-7. doi: 10.1016/j.joms.2004.05.207.
- Quinones-Hinojosa A, Ware ML, Sanai N, McDermott MW. Assessment of image guided accuracy in a skull model: comparison of frameless stereotaxy techniques vs. frame-based localization. J Neurooncol. 2006 Jan;76(1):65-70. doi: 10.1007/s11060-005-2915-z.
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- Watzinger F, Ewers R, Henninger A, Sudasch G, Babka A, Woelfl G. Endosteal implants in the irradiated lower jaw. J Craniomaxillofac Surg. 1996 Aug;24(4):237-44. doi: 10.1016/s1010-5182(96)80007-2.
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- Weischer T, Mohr C. Implant-supported mandibular telescopic prostheses in oral cancer patients: an up to 9-year retrospective study. Int J Prosthodont. 2001 Jul-Aug;14(4):329-34.
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- Kooy HM, Dunbar SF, Tarbell NJ, Mannarino E, Ferarro N, Shusterman S, Bellerive M, Finn L, McDonough CV, Loeffler JS. Adaptation and verification of the relocatable Gill-Thomas-Cosman frame in stereotactic radiotherapy. Int J Radiat Oncol Biol Phys. 1994 Oct 15;30(3):685-91. doi: 10.1016/0360-3016(92)90956-i.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. september 2007
Primær færdiggørelse (Forventet)
1. december 2011
Studieafslutning (Forventet)
1. december 2011
Datoer for studieregistrering
Først indsendt
2. juni 2009
Først indsendt, der opfyldte QC-kriterier
19. juni 2009
Først opslået (Skøn)
22. juni 2009
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
22. juni 2011
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
21. juni 2011
Sidst verificeret
1. juni 2011
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- ET2006-032
- CPP 07/033 [UBET83]
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .