Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06455540

SUperior Hypogastric Plexus Block During Laparoscopic hysterEctomy (SUBTLE)

Superior Hypogastric Plexus Block During Laparoscopic Hysterectomy

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
198 (estimated)
Sponsor
Sixth Affiliated Hospital, Sun Yat-sen University · Academic / Other
Sex
Female
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This trial sest to assess the efficacy of a superior hypogastric plexus block (SHPB) for quality of recovery after a laparoscopic hysterectomy.

Conditions

Interventions

TypeNameDescription
PROCEDURESuperior hypogastric plexus blockPrior to the laparoscopic hysterectomy and any additional procedures, the superior hypogastric plexus block will be performed on all the patients. The block will contain 20 mL of 0.75% ropivacaine hydrochloride or 0.9% normal saline. The injection will be performed by tenting the presacral peritoneum, aspirating with a laparoscopic needle-tip syringe to ensure extravascular placement, and injecting the block.

Timeline

Start date
2024-07-16
Primary completion
2025-07-15
Completion
2025-12-31
First posted
2024-06-12
Last updated
2024-06-14

Source: ClinicalTrials.gov record NCT06455540. Inclusion in this directory is not an endorsement.