Mode
Text Size
Log in / Sign up
N/A Completed N=78

Superior Hypogastric Blockade for Postoperative Pain

Superior Hypogastric Plexus Block · Hysterectomy · Pain, Postoperative · Gynecologic Disease
Source: ClinicalTrials.gov NCT03428152 ↗
Enrolled (actual)
78
Serious AEs
0.0%
Results posted
Jun 2019
Primary outcomePrimary: Postoperative Pain Scores — 4.76; 7.38; 3.7; 6.66 units on a scale

Summary

The primary indication for superior hypogastric (SHP) block is visceral pelvic pain, most commonly from malignancy of the ovary, uterus, cervix, bladder, rectum or prostate. Percutaneous SHP blocks should be done under guidance of ultrasonography, fluoroscopy, magnetic resonance or computed tomography. Because of the close proximity of SHP to major vessels, and structures like vertebral column (for posterior) and guts (for anterior) are being on the way of the needle, these percutaneous blocks are associated with serious complications. Performing SHP during hysterectomy surgery, gives advantages to rule out these complications by exploring the whole intraabdominal anatomy. The investigators' theory is to find out if SHP blocks (during pelvic surgery) are useful for decreasing VAS pain scores and opioid consumption for postoperative pain.

Outcome Measures

OutcomeResultp-value
PRIMARY
Postoperative Pain Scores
4.76; 7.38; 3.7; 6.66; 1.9; 4.23
PRIMARY
Postoperative Analgesic Consumption
0.8; 0.96; 0.1; 0.36; 2.83; 5.77
SECONDARY
Rescue Analgesic Time
627; 203.83
SECONDARY
Duration of Operation
115.83; 114.16
SECONDARY
Length of Hospital Stay
2.66; 2.96
SECONDARY
Number of Participants With Complications Due to SHP Block
7; 8; 0; 0

Eligibility Criteria

Inclusion Criteria

  • ASA I - II
  • Elective hysterectomy

Exclusion Criteria

  • ASA III
  • Different kind of surgery
  • Known allergy to local anesthetic drugs
  • Different analgesia protocol (ie: epidural, TAP block,..)
  • Refusal of the patient
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03428152). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

Back to search