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Single-port Versus Multi-port Laparoscopic Surgery for Ectopic Pregnancy

Effectiveness and Safety of Single-port Versus Multi-port Laparoscopic Surgery in the Treatment of Ectopic Pregnancy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05890066
Enrollment
100
Registered
2023-06-06
Start date
2023-11-01
Completion date
2024-05-31
Last updated
2023-06-07

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

Conditions

Ectopic Pregnancy

Keywords

Laparoscopic surgery, Single-port laparoscope, Multi-port laparoscope

Brief summary

This study aims to compare the effectiveness and Safety of Single-port Versus Multi-port Laparoscopic Surgery in the Treatment of Ectopic Pregnancy

Detailed description

Single-port laparoscopic surgery has become one of the treatment options for ectopic pregnancy with certain advantages such as reduced numbers of incision and scars, and increased patient's satisfaction post-surgery. At Hung Vuong hospital, the investigators do not have data about the application potential of single-port laparoscopic surgery for ectopic pregnancy treatment. Therefore, the investigators carry out this project to compare the effectiveness and safety of single-port versus traditional multi-port laparoscopic surgery in the treatment of ectopic pregnancy.

Interventions

PROCEDUREsingle-port laparoscopy

Compare the effectiveness and safety between single-port and multi-port laparoscopic surgery

Sponsors

Hung Vuong Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

The study is a parallel-group randomized control trial with 2 arms. Arm 1 includes patients who will be treated by traditional multi-port laparoscopic surgery. Aim 2 includes patients who will be treated by single-port laparoscopic surgery. All patients are randomized using computer-generated sequences with allocation ratio 1:1. This is a non-blinded study where all patients and surgical teams know the treatment option.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years old or older pregnant women who are indicated for laparoscopic surgery in the treatment of ectopic pregnancy. * Agree to participate and give a consent

Exclusion criteria

* Allergic reactions to anesthetics * Hemodynamic instability * Ruptured ectopic pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Blood lossImmediately post surgeryMeasure the amount of blood loss
Surgical timeImmediately post surgeryHow long will it take for single-port vs multi-port surgical procedures

Secondary

MeasureTime frameDescription
Pain intensityWithin 4 weeks post surgeryUse visual analogue scale to measure
Surgical complicationsWithin 4 weeks post surgeryOrgan damages, surgical site infections, pneumoperitoneum
Hospital stayWithin 4 weeks post surgeryHow long will be the recovery time

Contacts

Primary ContactTri B Nguyen, Doctor
ngoc.lam@ttu.edu.vn0983739959
Backup ContactNGOC T LAM, PhD

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026