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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02428257
Other study ID # P-2015008AR
Secondary ID
Status Not yet recruiting
Phase N/A
First received April 23, 2015
Last updated April 27, 2015
Start date June 2015
Est. completion date December 2015

Study information

Verified date April 2015
Source Institut Kassab d'Orthopédie
Contact Karim Raies, A. Professor
Phone +21655208602
Email karim.raies@gmail.com
Is FDA regulated No
Health authority Tunisia: Ministry of Public Health
Study type Interventional

Clinical Trial Summary

The study evaluates the potential beneficial effects on hemodynamics when hypobaric bupivacaine is used instead of isobaric bupivacaine in continuous spinal anesthesia for surgical repair of hip fracture in elderly patients. Half of the patients will receive hypobaric bupivacaine and the over half will reveive isobaric bupivacaine and hemodynamic data will be compared.


Description:

Anesthesia for surgical repair of hip fracture is still controversial. Large retrospective studies and systematic reviews failed to demonstrate the superiority of either general or regional anesthesia. However, continuous spinal anesthesia has been shown to preserve hemodynamics better than general and single shoot spinal anesthesia. However, hypotension still occurs with continuous spinal anesthesia.

Unilateral spinal anesthesia may be achieved by hypobaric bupivacaine when patients are in the lateral position. Unilateral spinal anesthesia is more effective in preserving hemodynamics by limiting the spread of the sympathetic blockade to the operated side.

Our goal is to show that the use of hypobaric rather than isobaric bupivacaine in continuous spinal anesthesia for surgical repair of hip fracture reduces incidence of hypotension.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 120
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Patients aged more than 65 years and scheduled for a surgical repair of a hip fracture.

Exclusion Criteria:

- contraindication to spinal anesthesia or peripheral nerve blocks including hemostasis anomalies, local infection, allergic reaction to local anesthetics.

- dementia.

- consent refusal.

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Procedure:
continuous spinal anesthesia
Spinal puncture performed with a 19-gauge Tuohy needle at the L4-L5 or L3-L4 interspace using a midline approach. 3 cm of a 22-gauge catheter introduced through the needle, directed to the fractured side.
Drug:
hypobaric bupivacaine
hypobaric bupivacaine was prepared diluting each 1 ml of 0.5% isobaric bupivacaine with 1 ml of sterile water.
isobaric bupivacaine
0.5% isobaric bupivacaine
ephedrine


Locations

Country Name City State
Tunisia Institut Kassab d'Orthopédie La Manouba

Sponsors (1)

Lead Sponsor Collaborator
Institut Kassab d'Orthopédie

Country where clinical trial is conducted

Tunisia, 

References & Publications (3)

Minville V, Fourcade O, Grousset D, Chassery C, Nguyen L, Asehnoune K, Colombani A, Goulmamine L, Samii K. Spinal anesthesia using single injection small-dose bupivacaine versus continuous catheter injection techniques for surgical repair of hip fracture — View Citation

Neuman MD, Rosenbaum PR, Ludwig JM, Zubizarreta JR, Silber JH. Anesthesia technique, mortality, and length of stay after hip fracture surgery. JAMA. 2014 Jun 25;311(24):2508-17. doi: 10.1001/jama.2014.6499. — View Citation

Patorno E, Neuman MD, Schneeweiss S, Mogun H, Bateman BT. Comparative safety of anesthetic type for hip fracture surgery in adults: retrospective cohort study. BMJ. 2014 Jun 27;348:g4022. doi: 10.1136/bmj.g4022. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The percentage of patients who experienced at least one episode of hypotension during surgery (fall of more than 20% of systolic blood pressure) among the 2 groups 2 hours Yes
Secondary Total bupivacaine consumption total dose of bupivacaine needed to perform the surgery (approximate duration of surgery : 2 hours) 2 hours No
Secondary The percentage of patients who experienced at least one episode of bradycardia (heart rate<50 bpm) among the 2 groups 2 hours Yes
Secondary vasopressor use total ephedrine injected if hypotension occurred (approximate duration of surgery : 2 hours). 2 hours Yes
Secondary fluid infusion total fluid infused intravenously at the end of surgery (approximate duration of surgery : 2 hours). 2 hours No
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