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MIS-TLIF Intraoperative Nerve Block Combined with No Placement of Drainage to Optimize Postoperative Effect and Promote Early Recovery of Lumbar Disc Herniation: A Prospective Non-Randomized Controlled Trial

MIS-TLIF Intraoperative Nerve Block Combined with No Placement of Drainage to Optimize Postoperative Effect and Promote Early Recovery of Lumbar Disc Herniation: A Prospective Non-Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016236
Enrollment
Unknown
Registered
2018-05-21
Start date
2018-05-10
Completion date
Unknown
Last updated
2018-05-28

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

Conditions

Middle-aged person with lumbar disc herniation

Interventions

PRP group:Application of gelatin sponge impregnated with a mixture of 3 drugs to intraoperative nerve root block
Control group:Gelatin sponge impregnated with saline and no drainage tube placed after surgery

Sponsors

Hong-hui Hospital, Xi'an Jiaotong University College of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. imaging examination prompted lumbar disc herniation; 2. Patients had typical symptoms of nerve roots, conservative treatment was ineffective and therefore had surgical indications; 3. middle-aged patients (age 45-60 years old); 4. posterolateral lumbar disc herniation, central lumbar disc herniation without calcification, suitable for MIS-TLIF surgery; 5. a single segmental herniated disc and is a limb of the root; 6. Postoperative CT examination excluded screw-related neurological complications; 7. Failure to incorporate other diseases that may cause lower extremity pain.

Exclusion criteria

Exclusion criteria: 1. combined with intervertebral space infection or postoperative wound infection 2. unstable segment of intervertebral disc, huge herniated intervertebral disc, difficult to open the window, central stenosis, extreme lateral disc herniation; 3. The patient's pain threshold is too low or psychological instability can not be assessed; 4. history of previous spinal surgery, secondary surgery may be associated with nerve root adhesions; 5. The skin test before surgery is allergic to the drug mixture; 6. Patients who use pain pump or intramuscular injection after surgery; 7. pregnant patients.

Design outcomes

Primary

MeasureTime frame
VAS scores of lower limb pain before and 1-10 days after surgery;Length of bed after surgery;Length of hospital stay;

Secondary

MeasureTime frame
Preoperative and postoperative 1-10 days low back pain VAS score;Preoperative and postoperative 3, 6-day JOA score;The incidence of thrombotic complications;The incidence of postoperative nerve root edema reactive pain ;Postoperative satisfaction survey results;

Countries

China

Contacts

Public ContactDing-Jun Hao

Hong-hui Hospital, Xi'an Jiaotong University College of Medicine

hhyyhdj@126.com+86 13909297839

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 24, 2026