Experimental cohort study on laparoscopic mesh removal for otherwise intractable inguinal pain after endoscopic hernia repair

Laparoscopic mesh removal for groin pain

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON27584

Enrollment

Registered

2019-08-15

Start date

2019-06-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

CPIP

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: all 44 consecutive patients who had undergone laparoscopic mesh removal for chronic postoperative inguinal pain (CPIP) at the expertisecenter for abdominal wall and groin pain from August 2014 to February 2019.

Exclusion criteria

Exclusion criteria: Mesh allergy Bilateral mesh removal

Design outcomes

Primary

Measure	Time frame
Pain intensity on Numeric Rating Score (NRS)	—

Secondary

Measure	Time frame
QoL: Brief Pain Inventory, Short Form-12 Patient satisfaction Recurrence rate of hernia Postoperative complications	—

Contacts

Public ContactChristel Perquin

Maxima Medisch Centrum

christel.perquin@mmc.nl31627022685

Outcome results