Pain reduction for TAPP-technique using perioperative rectus sheath block

Pain reduction for TAPP-technique using perioperative rectus sheath block - STOPR-trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00032750

Enrollment

Registered

2023-09-26

Start date

2023-10-30

Completion date

Unknown

Last updated

2025-10-06

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

Conditions

K40

Interventions

Group 1: All patients receive standardized anesthesia management according to the following protocol: Premedication: Etoricoxib (Arcoxia®), 60mg p.o. Ondansetron 8mg p.o. Dexamethasone 8mg p.o. Anes

Eligibility

Sex/Gender

Male

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: single side hernia surgery in TAPP- (Transabdominal Preperitoneal) technique

Exclusion criteria

Exclusion criteria: - No planned hernia surgery - Bilateral hernia surgery - Expansion of the intervention - Other surgical technique - Inability to understand or answer the questions - Allergy to one of the medications used

Design outcomes

Primary

Measure	Time frame
Postoperative pain 3h after surgery	—

Secondary

Measure	Time frame
- Postoperative pain in the first 24 hours - Procedure-specific complications within 30 days - Quality of life resulting from this intervention	—

Countries

Germany

Contacts

Public ContactJonas Herzberg

Krankenhaus Reinbek St. Adolf-Stift

jonas.herzberg@krankenhaus-reinbek.de+494072805375

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026