Effects of Alpha-1 Antagonist, Stress and Relaxation on Anorectal Functions



Status:Completed
Conditions:Constipation
Therapuetic Areas:Gastroenterology
Healthy:No
Age Range:18 - 80
Updated:1/31/2019
Start Date:March 2013
End Date:September 6, 2017

Use our guide to learn which trials are right for you!

Effect of Stress and a Alpha-1 Antagonist on Anorectal Functions

This study is designed to better understand the effects of effects of stress, relaxation, and
a medication alfuzosin on bowel control and emptying in healthy people and patients with
bowel problems.

Normally, bowel emptying requires relaxation of the anal sphincter (i.e., lowermost end of
intestinal tract) and pelvic muscles. Some people cannot relax these muscles normally and
experience constipation. Alfuzosin is a medication which is approved to treat bladder but not
bowel problems.

Inclusion criteria for controls (Part A only):

- Healthy

- Able to provide written informed consent before participating in the study

- Able to communicate adequately with the investigator and to comply with the
requirements for the entire study.

Inclusion criteria for patients (Parts A and B):

- Women with chronic constipation for 1 year with any 2 or more of the following
symptoms for 3 months or longer, i.e. <3 bowel motions/week, straining ≥ 25% of time,
hard or lumpy stools ≥ 25% of time, incomplete evacuation ≥ 25% of time, feeling of
anorectal blockage ≥ 25% of time.

- Able to provide written informed consent before participating in the study

- Able to communicate adequately with the investigator and to comply with the
requirements for the entire study.

Exclusion criteria for controls (Part A); Items indicated with an asterisk (*) are also
exclusion criteria for patients (Parts A and B):

- Clinical evidence of significant cardiovascular, respiratory, renal, hepatic,
gastrointestinal, hematological, neurological, psychiatric or other disease that may
interfere with the objectives of the study and/or pose safety concerns.*

- Current symptomatic orthostatic hypotension or history of hypotensive response as
defined by a reduction of ≥ 30 mmHg in systolic or ≥ 20 mmHg in diastolic blood
pressure.*

- Current symptoms of a functional gastrointestinal disorder assessed by questionnaire.

- Putative risk factors for pelvic floor trauma, i.e. six or more vaginal deliveries,
birthweight >4500gms (macrosomia), or known 4th degree perineal tear.

- Inability to withdraw medications prior to the baseline period and throughout the
study (except as protocol defined rescue medications):

1. Medications that substantially alter GI transit* including laxatives, magnesium
and aluminum containing antacids, prokinetics, erythromycin, narcotics,
anti-cholinergics, tricyclic antidepressants, serotonin-norepinephrine reuptake
inhibitors (SNRI) and newer antidepressants

2. Selective serotonin reuptake inhibitor (SSRI) antidepressants are permissible at
low, stable doses. All medications shall be reviewed and dis/approved by the
principal investigator on a case by case basis.*

3. Potent Cytochrome P450 3A4 (Cyp3A4) inhibitors such as ketoconazole, itraconazole
and ritonavir, nitrates and phosphodiesterase inhibitors.* Note: stable doses of
thyroid replacement, estrogen replacement, low dose aspirin for cardioprotection,
and birth control (but with adequate backup contraception as drug-interactions
with birth control have not been conducted) are permissible.*

- Stable dose of thyroxine will be permitted*

- Prolonged Q-Tc interval > 500 msec on ECG within the last three months*

- Estimated glomerular filtration rate (eGFR) < 60 mL/minute. * Based on guidelines and
recommendations from the National Kidney Disease Education Program (NKDEP) of the
National Institutes of Health (NIH) and the Kidney Disease Outcomes Quality Initiative
(KDOQI) of the National Kidney Foundation, the an eGFR using the Modification of Diet
in Renal Disease (MDRD) Study equation is more accurate than a creatinine clearance
calculated from serum and urine measurements. The formula is eGFR (mL/min/1.73 m2) =
175 x (Scr)-1.154 x (Age)-0.203 x (0.742 if female) x (1.210 if African American).
Based on our extensive experience in clinical practice and research studies, it is
anticipated that all potentially eligible participants will have normal serum
creatinine.

- History of allergies to alpha-1 adrenoreceptor antagonist*

- Active rectal inflammation, cancer; perianal sepsis; history of pelvic radiation,
rectosigmoid surgery or inflammatory bowel disease*

- Pregnant women, prisoners and institutionalized individuals*

- Persons with a latex allergy.
We found this trial at
1
site
200 First Street SW
Rochester, Minnesota 55905
507-284-2511
Phone: 507-255-2783
Mayo Clinic Rochester Mayo Clinic is a nonprofit worldwide leader in medical care, research and...
?
mi
from
Rochester, MN
Click here to add this to my saved trials