UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000042506
Receipt number R000047849
Scientific Title Effects of manual therapy on peripheral neuropathy after spinal fusion surgery -Comparison of the two types of manual therapy-: Randomized controlled trial
Date of disclosure of the study information 2020/12/01
Last modified on 2022/11/21 22:05:40

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Effects of rehabilitation on pain and numbness after spinal fusion surgery

Acronym

Effects of rehabilitation

Scientific Title

Effects of manual therapy on peripheral neuropathy after spinal fusion surgery -Comparison of the two types of manual therapy-: Randomized controlled trial

Scientific Title:Acronym

Effects of manual therapy

Region

Japan


Condition

Condition

After spinal surgery

Classification by specialty

Orthopedics Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To compare the effects of neuromobilization and soft tissue mobilization on neurological symptoms after spinal fusion surgery.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Visual Analog Scale

Key secondary outcomes

JOABPEQ
SLR Test
pain DETECT


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Nerve Mobilization

Interventions/Control_2

Soft Tissue Mobilization

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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

After spinal fusion surgery

Key exclusion criteria

Medical disorders related to peripheral neuropathy
Dimentia
A diagnosed neurological disorder
The appearance of post-operative delirium
Post-operative complications

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Takumi
Middle name
Last name Nakamura

Organization

Sanraku Hospital

Division name

Orthopedics

Zip code

101-0062

Address

Tokyo, Chiyoda-ku, Kandasurugadai, 2-5

TEL

03-3292-3981

Email

nkmrtkm1625aauaaui@icloud.com


Public contact

Name of contact person

1st name Takumi
Middle name
Last name Nakamura

Organization

Sanraku Hospital

Division name

Orthopedics

Zip code

101-0062

Address

Tokyo, Chiyoda-ku, Kandasurugadai, 2-5

TEL

03-3292-3981

Homepage URL


Email

nkmrtkm1625aauaaui@icloud.com


Sponsor or person

Institute

Sanraku Hospital Orthopedics

Institute

Department

Personal name



Funding Source

Organization

nothing

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Sanraku Hospital

Address

Tokyo, Chiyoda-ku, Kandasurugadai, 2-5

Tel

03-3292-3981

Email

nkmrtkm1625aauaaui@icloud.com


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

Institutions



Other administrative information

Date of disclosure of the study information

2020 Year 12 Month 01 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Open public recruiting

Date of protocol fixation

2020 Year 10 Month 01 Day

Date of IRB

2020 Year 10 Month 16 Day

Anticipated trial start date

2020 Year 12 Month 01 Day

Last follow-up date

2021 Year 12 Month 31 Day

Date of closure to data entry

2021 Year 12 Month 31 Day

Date trial data considered complete

2021 Year 12 Month 31 Day

Date analysis concluded

2021 Year 12 Month 31 Day


Other

Other related information



Management information

Registered date

2020 Year 11 Month 19 Day

Last modified on

2022 Year 11 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000047849


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name