Cervical Interfascial Plane (CIP) block

Cervical Interfascial Plane (CIP) block for postoperative analgesia following cervical spine surgery: a prospective randomized controlled trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201811665246016

Enrollment

Registered

2018-11-26

Start date

2018-12-01

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

analgesia for cervical spine surgery

Interventions

control

Cervical Interfascial Plane block

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: aged 18-60 years either gender ASA I-II undergoing elective cervical spine surgery

Exclusion criteria

Exclusion criteria: Patient refusal patients with any contraindication to regional anesthesia (e.g. local infection, coagulation abnormality) known allergy to local anesthetics mental disorders drug or alcohol abuse

Design outcomes

Primary

Measure	Time frame
VAS at 2h postoperative	—

Secondary

Measure	Time frame
intraoperative fentanyl consumption;postoperative rescue pethidine consumption.	—

Countries

Egypt

Contacts

Public ContactShaimaa Farouk

lecturer of anesthesia and surgical ICU Tanta University Faculty of Medicine

shaimaafarouk7777@yahoo.com+201270440771

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026