UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020413
Receipt number R000023573
Scientific Title Measuring skin to subarachnoid space depth in Egyptian population, A prospective cohort study.
Date of disclosure of the study information 2016/01/04
Last modified on 2016/01/18 01:19:43

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Basic information

Public title

Measuring skin to subarachnoid space depth in Egyptian population, A prospective cohort study.

Acronym

Measuring skin to subarachnoid space depth in Egyptian population, A prospective cohort study.

Scientific Title

Measuring skin to subarachnoid space depth in Egyptian population, A prospective cohort study.

Scientific Title:Acronym

Measuring skin to subarachnoid space depth in Egyptian population, A prospective cohort study.

Region

Africa


Condition

Condition

This study tries to measure the skin to subarachniod distance in Egyptian population generally and in individual male, females and pregnant females and find a differences between them

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

to measure the skin to subarachnoid distance in Egyptian population

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

to know the skin to subarachnoid distance in egyptian population and put a formula for its calculation by approach the subarachniod space in midline by a spinal needle and put a mark on that needle and measure a distance by a ruler and find a correlation between it and bodymass index

Key secondary outcomes

to find which formula is applicable in egyptian population


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

Diagnosis

Type of intervention

Maneuver

Interventions/Control_1

we insert a spinal needle in l3-4 space and measure the distance from skin to subarachnoid space using a spescific measurement

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

18 years-old <=

Age-upper limit

60 years-old >=

Gender

Male and Female

Key inclusion criteria

400 adult Egyptian patients (age is 18- 60byears) of either sex, ASA I&II, who will submitted for elective surgical procedures under spinal anesthesia

Key exclusion criteria

Patients with neurological disorder, history of seizures, spinal anomaly, low back pain, prior back surgery, skin infection at puncture site, sepsis, drug allergies and coagulation defects will be excluded. Pregnant females with hypertensive disorder, less than term pregnancy or those scheduled for surgery other than caesarean delivery

Target sample size

400


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hani I, Taman

Organization

Mansoura faculty of medicine, anestheasia department

Division name

Mansoura university main hospital

Zip code


Address

17, elgomhoria street, mansoura, egypt

TEL

+81-2050220772

Email

hani_taman@mans.edu.eg


Public contact

Name of contact person

1st name
Middle name
Last name Hani I, Taman

Organization

Mansoura faculty of medicine, anestheasia department

Division name

Mansoura university main hospital

Zip code


Address

17 elgomhoria street, mansoura, egypt

TEL

+81-2050220772

Homepage URL


Email

hani_taman@mans.edu.eg


Sponsor or person

Institute

Mansoura Faculty of Medicine

Institute

Department

Personal name



Funding Source

Organization

Self funding

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

2016 Year 01 Month 04 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

Completed

Date of protocol fixation

2014 Year 12 Month 08 Day

Date of IRB


Anticipated trial start date

2015 Year 01 Month 02 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 01 Month 01 Day

Last modified on

2016 Year 01 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023573


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name