| Recruitment status | Completed |
| Unique ID issued by UMIN | UMIN000023442 |
| Receipt No. | R000026968 |
| Official scientific title of the study | Phase II trial of Transcatheter arterial micro-embolization for refractory chronic knee pain: Multicenter Study (PATRICK study) |
| Date of disclosure of the study information | 2016/08/03 |
| Last modified on | 2018/05/08 (Ver. 3) |
| Basic information | ||
| Official scientific title of the study | Phase II trial of Transcatheter arterial micro-embolization for refractory chronic knee pain: Multicenter Study (PATRICK study) | |
| Title of the study (Brief title) | knee TAME: JMIS-1602 (PATRICK study) | |
| Region |
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| Condition | |||
| Condition | chronic knee pain refractory to non-surgical management due to mild osteoarthritis or after artificial joint replacement | ||
| Classification by specialty |
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| Classification by malignancy | Others | ||
| Genomic information | NO | ||
| Objectives | |
| Narrative objectives1 | Phase II trial of Transcatheter arterial micro-embolization for refractory chronic knee pain: Multicenter Study (PATRICK study) |
| Basic objectives2 | Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | Phase II |
| Assessment | |
| Primary outcomes | Numerical Rating Scale (NRS) in 6 months after procedure
Japanese knee osteoarthritis measure(JCOM) score in 6 months after procedure Quality of Life(QOL) in 6 months after procedure |
| Key secondary outcomes | |
| Base | |
| Study type | Interventional |
| Study design | |
| Basic design | Single arm |
| Randomization | Non-randomized |
| Randomization unit | |
| Blinding | Open -no one is blinded |
| Control | Uncontrolled |
| Stratification | |
| Dynamic allocation | |
| Institution consideration | |
| Blocking | |
| Concealment | |
| Intervention | ||
| No. of arms | 1 | |
| Purpose of intervention | Treatment | |
| Type of intervention |
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| Interventions/Control_1 | Transcatheter arterial micro embolization: TAME | |
| Interventions/Control_2 | ||
| Interventions/Control_3 | ||
| Interventions/Control_4 | ||
| Interventions/Control_5 | ||
| Interventions/Control_6 | ||
| Interventions/Control_7 | ||
| Interventions/Control_8 | ||
| Interventions/Control_9 | ||
| Interventions/Control_10 | ||
| Eligibility | ||||
| Age-lower limit |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | 1.Previous conservative therapies applied for at least 3 months and persistent moderate-to-severe knee pain (NRS>=5).
2.Chronic knee pain with mild osteoarthritis or after artificial joint replacement 3.Patients with no severe knee osteoarthritis (Kellgren-Lawrence grading system 0-2) 4.Patients with maintain major organ (bone marrow, heart, liver, lung, kidney) function. 5.Patients with possibility of going to hospital and follow up for 6 months. 6.Provided written informed consent to undergo the procedure. |
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| Key exclusion criteria | 1.Surgical candidate
2.Patients with severe infection, rheumatoid arthritis, or mental disorder 3.Patients with uncontrollable diabetic mellitus 4.Pain due to spine pathology 5.Patients with osteonecrosis with magnetic resonance imaging (MRI) 6.Patients without possibility of going to hospital and follow up for 6 months. 7.Patient who was decided not to be appropriate for this trial by physician |
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| Target sample size | 50 | |||
| Research contact person | |
| Name of lead principal investigator | Taku Yasumoto |
| Organization | Miyakojima IGRT clinic |
| Division name | Department of Interventional Radiology |
| Address | 1-16-22 Miyakojima Hondori, Miyakojima-ku, Osaka, 534-0021, JAPAN |
| TEL | 06-6923-3501 |
| yasumoto@solid.ocn.ne.jp | |
| Public contact | |
| Name of contact person | Taku Yasumoto |
| Organization | Miyakojima IGRT clinic |
| Division name | Department of Interventional Radiology |
| Address | 1-16-22 Miyakojima Hondori, Miyakojima-ku, Osaka, 534-0021, JAPAN |
| TEL | 06-6923-3501 |
| Homepage URL | |
| yasumoto@solid.ocn.ne.jp | |
| Sponsor | |
| Institute | Miyakojima IGRT clinic |
| Institute | |
| Department | |
| Funding Source | |
| Organization | None |
| Organization | |
| Division | |
| Category of Funding Organization | Self funding |
| Nationality of Funding Organization | |
| Other related organizations | |
| Co-sponsor | |
| Name of secondary funder(s) | |
| Secondary IDs | |
| Secondary IDs | NO |
| Study ID_1 | |
| Org. issuing International ID_1 | |
| Study ID_2 | |
| Org. issuing International ID_2 | |
| IND to MHLW | |
| Institutions | |
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| Date of disclosure of the study information |
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| Progress | |||||||
| Recruitment status | Completed | ||||||
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| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| URL releasing results | |
| Results | |
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| Management information | |||||||
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026968 |