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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03221686
Other study ID # H-15017272
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 20, 2016
Est. completion date December 10, 2017

Study information

Verified date July 2017
Source Bispebjerg Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Collagen synthesis is depressed systemically in the immediate postoperative period. Arginine, zinc and vitamin C impact collagen synthesis.

The aim of this study is to investigate the effect of a pre and postoperative oral supplement consisting of arginine, zinc and vitamin C on collagen synthesis in patients undergoing inguinal hernia repair.


Description:

The trial investigates the effect of a pre and postoperative oral supplement consisting of arginine, zinc and vitamin C on collagen type I synthesis in patients undergoing inguinal hernia repair.

The patients in the intervention group are given 55 mg zinc, 1251 mg vitamin C, and 15 g arginine once daily 14 days pre-operatively and post-operatively. Both groups receive high quality protein (1.5 g protein/kg body weight) daily during the same period. Hernia repair is done using the Lichtenstein technique. Drainage tubes are placed in the wound during the surgery. Epidermal wounds (10 mm) are made via the suction blister method on the ventral forearm of the patients on the day of surgery. Blood samples are drawn at day -14, day 0, day 1 and day 2. The surgical drain is emptied and fluid collected at day 1 and day 2.The healing of the suction blisters is assessed by clinical criteria until healing.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 10, 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age above 18 years

- Patients undergoing hernia repair using the Lichtenstein technique

- Written informed consent

Exclusion Criteria:

- Former surgery in the same area within 5 years

- Dementia

- Dysregulated diabetes

- Systemic corticosteroid treatment

- Liver disease

- Kidney disease

- Cancer within 5 years

- Need of interpreter

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Intervention
The patients in the intervention group are given 55 mg zinc, 1251 mg vitamin C, and 15 g arginine once daily 14 days pre-operatively and post-operatively together with a high quality protein supplement.
Control
High quality protein supplement 14 days pre-operatively and post-operatively.

Locations

Country Name City State
Denmark Bispebjerg Hospital Copenhagen Copenhagen NV

Sponsors (1)

Lead Sponsor Collaborator
Lars Nannestad Jorgensen

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in CICP levels in serum. CICP is the biomarker of type I collagen synthesis (carboxy-terminal propeptide of type I procollagen) CICP is measured by enzyme-linked immunosorbent assay Day 2
Secondary Changes in CICP levels in wound fluid collected from surgical drain. CICP is the biomarker of type I collagen synthesis (carboxy-terminal propeptide of type I procollagen). CICP is measured by enzyme-linked immunosorbent assay Day 1 and day 2
Secondary Changes in CICP levels in wound fluid collected from suction blisters. CICP is the biomarker of type I collagen synthesis (carboxy-terminal propeptide of type I procollagen). CICP is measured by enzyme-linked immunosorbent assay Day 0
Secondary Changes in Zinc levels in serum Zinc is measured by direct spectrophotometry Day -14, day 0, day 1 and day 2
Secondary Changes in Zinc levels in wound fluid collected from surgical drain Zinc is measured by direct spectrophotometry Day 1 and day 2
Secondary Changes in Zinc levels in wound fluid collected from suction blisters Zinc is measured by direct spectrophotometry Day 0
Secondary Changes in Arginine levels in serum Arginine is measure by ultra-performance liquid chromatography and mass spectrometry Day -14, day 0, day 1 and day 2
Secondary Healing of suction blisters Clinical assessment Day 3 to Suction Blister healing
Secondary Compliance Count of remaining supplement Day -14 to Suction Blister healing
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