Effectiveness of IV Vitamin C in Reducing Oxidative Stress Associated With Free Flap Surgery

U

University of Malaya

Status and phase

Enrolling
Phase 3

Conditions

Oxidative Stress
Ischemia-reperfusion Injury

Treatments

Drug: Normal Saline 10 mL Injection
Drug: Intravenous Ascorbate

Study type

Interventional

Funder types

Other

Identifiers

NCT05327348
PV042-2021 (Other Grant/Funding Number)
USM/JEPeM/21070522 (Other Identifier)
NMRR-21-1378-60482 (IIR) (Other Identifier)
MECID No,UMMC: 202086-8956

Details and patient eligibility

About

Ischemia and reperfusion injury during free flap reconstructive surgery creates a state of increased oxidative stress that can adversely affect the flap outcomes. Ascorbic acid (AA) had been proven to have beneficial effect on end-organ protection and flap survival from ischemia-reperfusion injury via its antioxidant properties. The investigators hypothesise that perioperative parenteral ascorbic acid treatment may reduce oxidative stress among participants undergoing free flap reconstructive surgery along with reduction in inflammatory markers, improved rate of flap viability and wound healing at both donor and recipient sites.

Full description

Temporary cessation of blood supply to the flap tissues from clamping of donor vascular pedicle (ischemia) followed by restoration of flap tissue perfusion (reperfusion) after micro-anastomosis are inevitable in any free flap surgery. In combination, the ischemia and reperfusion process during free flap tissue transfers induce a state of increased oxidative stress, which may lead to complications such as flap failure and non-healing wounds at either donor or recipient sites. The negative impacts of which include additional wounds from flap loss, higher costs and increased duration of hospital stay. Previous studies had demonstrated the beneficial effects of ascorbic acid in end-organ protection against ischemia and reperfusion injury. In addition, parenteral ascorbic acid has been shown to be remarkably safe even at high dose in both clinical and nonclinical models. Nonetheless, the data on efficacy of ascorbic acid in free flap survival in human is very limited. The aims of this prospective, multicentre, double-blind, randomized, placebo-controlled pilot study are to measure the extent of oxidative stress in participants undergoing free flap reconstructive surgery before and after administration of parenteral ascorbic acid; and to evaluate its efficacy on modulation of inflammation, flap viability and wound healing. Eligible participants will be randomized to receive 1 gram of parenteral ascorbic acid and 0.9% normal saline (as placebo) 8 hourly for 7 days (from pre-operative day 2 until post-operative day 5). Blood sampling will be performed on day 0 (pre-operative), day 3 (post-operative day 1) and day 5 (post-operative day 3) of intravenous ascorbic acid or placebo infusion for measurement of i) oxidative stress biomarkers, including isoprostane level, gene expression of glutamate-cystein ligase (GCL) and total glutathione level) ii) inflammatory markers, including leucocytes count and gene expression of TNF-α and IL-1. Post-operative outcomes of free flap surgery, up to post-operative 14 days, including flap viability, wound healing at both donor and recipient sites and duration of ICU and hospital stay will be evaluated. The investigators estimate that a total sample of 28 participants (14 on each arm) will be necessary for 80% power to detect a 33% oxidative stress reduction with medium effect size (0.5) at 5% level of significance (α) between treatment (intravenous ascorbic acid) and placebo group (0.9% normal saline). A total of 34 participants are required to account for 20% of dropouts. Primary analysis of this study utilizes an intention-to-treat approach and includes all randomized participants undergoing elective free flap reconstructive surgery. The mean difference between the baseline (pre-operative) and post-operative oxidative stress and inflammatory levels will be analyzed and compared between the intravenous ascorbic acid and placebo group using analysis of variance (ANOVA) for all normally distributed dataset whilst the non-parametric Kruskal-Wallis test is used, if otherwise. The effect size of such difference will be determined and compared. Subsequently, correlation between reduction of oxidative stress and post-operative flap outcomes in the intravenous ascorbic acid group will be evaluated. The secondary outcomes such as flap viability (percentage of flap necrosis), wound healing at both recipient and donor sites (percentage of wound dehiscence and percentage of skin graft failure to take/loss), duration of hospital and ICU stay and wound infection rate will be presented as mean with standard deviation (SD) or median with interquartile range (IQR) based on their normality distribution and are compared with Student's t-test or Mann-Whitney U test.

Enrollment

34 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults (age 18 years and older, male or female) who are planned for elective free flap reconstructive surgery.

Exclusion criteria

  • Hypersensitivity to vitamin C
  • Oliguria (urine output <400mL/day) or anuria (urine output <100mL/day)
  • Renal failure (serum creatinine level ≥175.0 %mol/L)
  • Hemodialysis
  • Renal calculi
  • Thalassemia
  • Glucose-6-phosphate dehydrogenase (G6PD) deficiency
  • Unfit for surgery
  • Pregnancy or lactating
  • Hemochromatosis
  • Hyperoxaluria

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

34 participants in 2 patient groups, including a placebo group

Parenteral Ascorbic Acid
Experimental group
Description:
Intravenous ascorbic acid 1 gram 8 hourly (3 grams per day) for 7 days
Treatment:
Drug: Intravenous Ascorbate
0.9% Normal Saline
Placebo Comparator group
Description:
Intravenous 0.9% normal saline 10 mL 8 hourly for 7 days
Treatment:
Drug: Normal Saline 10 mL Injection

Trial contacts and locations

3

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Central trial contact

Alizan B Abdul Khalil, MBBS; Raymond Yii Shi Liang, MBBS

Data sourced from clinicaltrials.gov

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