NCT02756156

Brief Summary

Combining interscalene block with infraclavicular block for humerus surgery provides a unique surgical anaesthesia and postoperative analgesia.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Apr 2016

Shorter than P25 for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 15, 2016

Completed
17 days until next milestone

Study Start

First participant enrolled

April 1, 2016

Completed
28 days until next milestone

First Posted

Study publicly available on registry

April 29, 2016

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2016

Completed
Last Updated

April 29, 2016

Status Verified

March 1, 2016

Enrollment Period

4 months

First QC Date

March 15, 2016

Last Update Submit

April 26, 2016

Conditions

Humerus Fracture

Keywords

interscaleneinfraclavicularhumerus surgery

Outcome Measures

Primary Outcomes (1)

  • Success rate of block

    A complete sensory loss in distribution of the radial, median, ulnar, musculocutaneous and medial cutaneous nerves of the arm

    10 min.- 20 min.

Secondary Outcomes (3)

  • Technique duration

    5 min.

  • Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

    24 hours

  • Complication rate

    24 hours

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients undergoing humerus surgery.

You may qualify if:

  • Patients accepting peripheral nerve block technique for humerus surgery
  • Unilateral orthopedic humerus surgery
  • years of age or older

You may not qualify if:

  • Patients refused peripheral nerve block
  • Non-cooperate patients
  • Neuropathy of any etiology in the affected extremity

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Humeral Fractures

Condition Hierarchy (Ancestors)

Arm InjuriesWounds and InjuriesFractures, Bone

Central Study Contacts

Bora Bilal, Asist. Prof.

CONTACT

+903442803245bilalbora@yahoo.com

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assist prof

Study Record Dates

First Submitted

March 15, 2016

First Posted

April 29, 2016

Study Start

April 1, 2016

Primary Completion

August 1, 2016

Study Completion

August 1, 2016

Last Updated

April 29, 2016

Record last verified: 2016-03

Data Sharing

IPD Sharing
Will not share